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Electrodeposition of Fe–Co Alloys into Nanoporous p-type Silicon: Influence of the Electrolyte Composition

Published online by Cambridge University Press:  31 January 2011

F. Hamadache
Affiliation:
Unité de Physico-Chimie et de Physique des Matériaux, Université Catholique de Louvain, Croix du Sud 1, B-1348 Louvain-la-Neuve, Belgique
J-L. Duvail
Affiliation:
Laboratoire de Physique Cristalline, Institut des Matériaux de Nantes, 2, Rue de la Houssinière, 44322 Nantes cedex 03, France
V. Scheuren
Affiliation:
Laboratoire de Microélectronique, Université Catholique de Louvain, Place du Levant 3, B-1348 Louvain-la-Neuve, Belgique
L. Piraux
Affiliation:
Unité de Physico-Chimie et de Physique des Matériaux, Université Catholique de Louvain, Croix du Sud 1, B-1348 Louvain-la-Neuve, Belgique
C. Poleunis
Affiliation:
Unité de Physico-Chimie et de Physique des Matériaux, Université Catholique de Louvain, Croix du Sud 1, B-1348 Louvain-la-Neuve, Belgique
P. Bertrand
Affiliation:
Unité de Physico-Chimie et de Physique des Matériaux, Université Catholique de Louvain, Croix du Sud 1, B-1348 Louvain-la-Neuve, Belgique
M. S. Belkaïd
Affiliation:
Laboratoire de Microélectronique Appliquée, Université Mouloud Mammeri de Tizi-Ouzou, Campus Universitaire Hasnaoua, 15000 Tizi-Ouzou, Algérie
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Extract

The cathodic deposition of iron–cobalt alloys inside the pores of anodically formed nanoporous silicon (PS) from p-type Si substrate is investigated with respect to the electrolyte composition. The samples were characterized by scanning electron microscopy, energy dispersive spectrometry, Auger electron spectroscopy, and Fourier transform infrared spectroscopy. Results showed that the nucleation of pure cobalt started at the bottom of the pores and the nucleation of pure iron occurred all over the pore walls, leading to a preferential deposition on top surface of the porous layer. Nevertheless, a low concentration of Co2+ ions (5 at.%) in the electrolyte drastically improved the penetration of iron into the pores. As a result, a good filling of the pores with Co metal as well as with Fe–Co alloys was achieved. It was also shown that the deposition process oxidizes the structure mainly at the pore walls. The results of our investigation indicate that the mechanisms occurring during the electrodeposition of metals on porous p-type silicon substrates are completely different depending on the kind of electrolyte used: pure iron-based electrolyte or cobalt-based solutions. A complete understanding of the deposition process requires further analyses of the carrier transport in PS and of the charge exchange at the Si/electrolyte and PS/electrolyte interfaces. These new results involving the deposition of iron-group materials into porous p-type silicon are useful for future silicon technologies.

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Copyright © Materials Research Society 2002

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