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Nanoscaled alloy formation from self-assembled elemental Co nanoparticles on top of Pt films

The thermally activated formation of nanoscale CoPt alloys was investigated, after deposition of self-assembled Co nanoparticles on textured Pt(111) and epitaxial Pt(100) films on MgO(100) and SrTiO(3)(100) substrates, respectively. For this purpose, metallic Co nanoparticles (diameter 7 nm) were pr...

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Autores principales: Han, Luyang, Wiedwald, Ulf, Biskupek, Johannes, Fauth, Kai, Kaiser, Ute, Ziemann, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3190617/
https://www.ncbi.nlm.nih.gov/pubmed/22003453
http://dx.doi.org/10.3762/bjnano.2.51
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author Han, Luyang
Wiedwald, Ulf
Biskupek, Johannes
Fauth, Kai
Kaiser, Ute
Ziemann, Paul
author_facet Han, Luyang
Wiedwald, Ulf
Biskupek, Johannes
Fauth, Kai
Kaiser, Ute
Ziemann, Paul
author_sort Han, Luyang
collection PubMed
description The thermally activated formation of nanoscale CoPt alloys was investigated, after deposition of self-assembled Co nanoparticles on textured Pt(111) and epitaxial Pt(100) films on MgO(100) and SrTiO(3)(100) substrates, respectively. For this purpose, metallic Co nanoparticles (diameter 7 nm) were prepared with a spacing of 100 nm by deposition of precursor-loaded reverse micelles, subsequent plasma etching and reduction on flat Pt surfaces. The samples were then annealed at successively higher temperatures under a H(2) atmosphere, and the resulting variations of their structure, morphology and magnetic properties were characterized. We observed pronounced differences in the diffusion and alloying of Co nanoparticles on Pt films with different orientations and microstructures. On textured Pt(111) films exhibiting grain sizes (20–30 nm) smaller than the particle spacing (100 nm), the formation of local nanoalloys at the surface is strongly suppressed and Co incorporation into the film via grain boundaries is favoured. In contrast, due to the absence of grain boundaries on high quality epitaxial Pt(100) films with micron-sized grains, local alloying at the film surface was established. Signatures of alloy formation were evident from magnetic investigations. Upon annealing to temperatures up to 380 °C, we found an increase both of the coercive field and of the Co orbital magnetic moment, indicating the formation of a CoPt phase with strongly increased magnetic anisotropy compared to pure Co. At higher temperatures, however, the Co atoms diffuse into a nearby surface region where Pt-rich compounds are formed, as shown by element-specific microscopy.
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spelling pubmed-31906172011-10-14 Nanoscaled alloy formation from self-assembled elemental Co nanoparticles on top of Pt films Han, Luyang Wiedwald, Ulf Biskupek, Johannes Fauth, Kai Kaiser, Ute Ziemann, Paul Beilstein J Nanotechnol Full Research Paper The thermally activated formation of nanoscale CoPt alloys was investigated, after deposition of self-assembled Co nanoparticles on textured Pt(111) and epitaxial Pt(100) films on MgO(100) and SrTiO(3)(100) substrates, respectively. For this purpose, metallic Co nanoparticles (diameter 7 nm) were prepared with a spacing of 100 nm by deposition of precursor-loaded reverse micelles, subsequent plasma etching and reduction on flat Pt surfaces. The samples were then annealed at successively higher temperatures under a H(2) atmosphere, and the resulting variations of their structure, morphology and magnetic properties were characterized. We observed pronounced differences in the diffusion and alloying of Co nanoparticles on Pt films with different orientations and microstructures. On textured Pt(111) films exhibiting grain sizes (20–30 nm) smaller than the particle spacing (100 nm), the formation of local nanoalloys at the surface is strongly suppressed and Co incorporation into the film via grain boundaries is favoured. In contrast, due to the absence of grain boundaries on high quality epitaxial Pt(100) films with micron-sized grains, local alloying at the film surface was established. Signatures of alloy formation were evident from magnetic investigations. Upon annealing to temperatures up to 380 °C, we found an increase both of the coercive field and of the Co orbital magnetic moment, indicating the formation of a CoPt phase with strongly increased magnetic anisotropy compared to pure Co. At higher temperatures, however, the Co atoms diffuse into a nearby surface region where Pt-rich compounds are formed, as shown by element-specific microscopy. Beilstein-Institut 2011-08-23 /pmc/articles/PMC3190617/ /pubmed/22003453 http://dx.doi.org/10.3762/bjnano.2.51 Text en Copyright © 2011, Han et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjnano/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Nanotechnology terms and conditions: (https://www.beilstein-journals.org/bjnano/terms)
spellingShingle Full Research Paper
Han, Luyang
Wiedwald, Ulf
Biskupek, Johannes
Fauth, Kai
Kaiser, Ute
Ziemann, Paul
Nanoscaled alloy formation from self-assembled elemental Co nanoparticles on top of Pt films
title Nanoscaled alloy formation from self-assembled elemental Co nanoparticles on top of Pt films
title_full Nanoscaled alloy formation from self-assembled elemental Co nanoparticles on top of Pt films
title_fullStr Nanoscaled alloy formation from self-assembled elemental Co nanoparticles on top of Pt films
title_full_unstemmed Nanoscaled alloy formation from self-assembled elemental Co nanoparticles on top of Pt films
title_short Nanoscaled alloy formation from self-assembled elemental Co nanoparticles on top of Pt films
title_sort nanoscaled alloy formation from self-assembled elemental co nanoparticles on top of pt films
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3190617/
https://www.ncbi.nlm.nih.gov/pubmed/22003453
http://dx.doi.org/10.3762/bjnano.2.51
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