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Electrochemical Deposition and Characterization of Ni in Mesoporous Silicon
Author(s) -
A L Dolgiy,
Sergey Redko,
Hanna Bandarenka,
S. L. Prischepa,
K. I. Yanushkevich,
Paolo Nenzi,
M. Balucani,
Vitaly Bondarenko
Publication year - 2012
Publication title -
journal of the electrochemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.258
H-Index - 271
eISSN - 1945-7111
pISSN - 0013-4651
DOI - 10.1149/2.050210jes
Subject(s) - materials science , nickel , porous silicon , silicon , mesoporous material , crystallite , nanowire , electrochemistry , magnetization , silicide , deposition (geology) , chemical engineering , nanotechnology , analytical chemistry (journal) , metallurgy , chemistry , electrode , paleontology , sediment , engineering , catalysis , biochemistry , physics , quantum mechanics , chromatography , magnetic field , biology
Nickel nanowires have been formed by stationary electrochemical deposition of nickel into mesoporous silicon templates from the modified Watts bath. Monitoring of the porous silicon potential during the electrochemical deposition has given the determination of the emergence of Ni on the outer surface of porous layer. Maximum filling factor of porous silicon with Ni has been achieved to 67%. The pore dimensions have been found to define the length and diameter of the Ni nanowires that have equaled to 10 mu m and 100-120 nm, respectively. The polycrystalline nature of the nickel nanowires, as well as the expansion of nickel lattice constant in comparison with bulk material has been established by analyzing the X-ray diffraction spectra. The synthesized samples have possessed ferromagnetic properties, which have been confirmed by temperature measurements of the magnetization. Smaller values of the specific magnetization of the Ni/PS samples and the atomic magnetic moment of Ni atoms at the low temperature with respect to those of bulk material have been suggested to be mostly caused by formation of nickel silicide at the beginning of the Ni electrochemical deposition. (C) 2012 The Electrochemical Society. [DOI: 10.1149/2.050210jes] All rights reserved

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