Nickel nanowires were synthesized via electroless deposition in an organic solvent (ethylene glycol) under a magnetic field. Deposition behavior of nickel particles and wires were electrochemically investigated at various concentrations of NaOH by an in-situ mixed potential measurement and voltammetry combined with quartz crystal microbalance. Based on the electrochemical investigation, a formation mechanism of nickel wires is proposed. According to the mechanism, nickel wires 100-370 nm in diameter with several dozen m of length were successfully prepared by controlling the reduction rate by varying a concentration of sodium hydroxide, trisodium citrate, and a nucleating agent, chloroplatinic acid.Nanowires of iron group metals (Fe, Co, Ni) and their alloys are attractive materials due to their magnetic properties. 1,2 Numerous synthesis methods of iron group nanowires have been reported. [3][4][5][6][7][8] In their methods, nanowires are formed by electrodeposition using templates such as anodized aluminum oxide 3-5 and polycarbonate membrane. 6-8 The methods with templates have notable advantages that highly-ordered and size-controlled nanowires can be obtained. The template methods, however, require several steps including fabrication and removal of templates in order to obtain bare nanowires. On the other hand, a self-assemble electroless deposition of ferromagnetic nanowires under a magnetic field is a relatively simple synthesis method without any templates. 9 In addition, electroless deposition is a powerful fabrication method with a wide variety of compositions and sizes in a large-scale 10,11 and thus, electroless deposition is suitable for a practical application.We have reported some studies of electrochemical approaches with in-situ mixed potential observation for the synthesis processes of copper, 12,13 cobalt, 14,15 nickel, 16 and Co-Ni alloy 17 nanoparticles, which is effective in thermodynamic oxidation-state control and analysis of the formation process of nanowires as well as nanoparticles. In the present work, the formation process of nickel nanowires via electroless deposition under a magnetic field was electrochemically investigated. In order to control the morphology of nickel deposits, the deposition behavior of nickel was studied by an in-situ mixed potential measurement; it is possible that the reduction rate of Ni(II) species affects the morphology of nickel deposits. Furthermore, the reduction rate and reduction potential of Ni(II) species were investigated by voltammetry combined with quartz crystal microbalance (QCM) as well as the oxidation rate and oxidation potential of hydrazine as a counterpart reaction.
ExperimentalThe reaction solutions were prepared using nickel chloride hexahydrate (NiCl 2 Á 6H 2 O) as a source of Ni(II) ions, ethylene glycol (EG) as a solvent, and hydrazine monohydrate (N 2 H 4 Á H 2 O) as a reducing agent. Sodium hydroxide (NaOH) was added as a source of OH À ions. Trisodium citrate dihydrate (Na 3 C 6 H 5 O 7 Á 2H 2 O) and chloroplatinic acid hexahydrate ...