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Pd@Fe2O3 Superparticles with Enhanced Peroxidase Activity by Solution Phase Epitaxial Growth

MPG-Autoren
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Simon,  Paul
Paul Simon, Chemical Metal Science, Max Planck Institute for Chemical Physics of Solids, Max Planck Society;

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Grin,  Juri
Juri Grin, Chemical Metal Science, Max Planck Institute for Chemical Physics of Solids, Max Planck Society;

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Zitation

Kluenker, M., Tahir, M. N., Ragg, R., Korschelt, K., Simon, P., Gorelik, T. E., et al. (2016). Pd@Fe2O3 Superparticles with Enhanced Peroxidase Activity by Solution Phase Epitaxial Growth. Chemistry of Materials, 29(3), 1134-1146. doi:10.1021/acs.chemmater.6b04283.


Zitierlink: https://hdl.handle.net/11858/00-001M-0000-002C-F779-5
Zusammenfassung
Compared to conventional deposition techniques for the epitaxial growth of metal oxide structures on a bulk metal substrate, wet-chemical synthesis based on a dispersible template offers advantages such as low cost, high throughput, and the capability to prepare metal/metal oxide nanostructures with controllable size and morphology. However, the synthesis of such organized multicomponent architectures is difficult because the size and morphology of the components are dictated by the interplay of interfacial strain and facet-specific reactivity. Here we show that solution-processable two-dimensional Pd nanotetrahedra and nanoplates can be used to direct the epitaxial growth of gamma-Fe2O3 nanorods. The interfacial strain at the Pd-gamma-Fe2O3 interface is minimized by the formation of an Fe Pd "buffer phase" facilitating the growth of the nanorods. The gamma-Fe2O3 nanorods show a (111) orientation on the Pd(111) surface. Importantly, the Pd@gamma-Fe2O3 hybrid nanomaterials exhibit enhanced peroxidase activity compared to that of isolated Fe2O3 nanorods with comparable surface area because of a synergistic effect for the charge separation and electron transport. The metal-templated epitaxial growth of nanostructures via wet-chemical reactions appears to be a promising strategy for the facile and high-yield synthesis of novel functional materials.