Journal of Industrial and Engineering Chemistry, Vol.13, No.2, 279-286, March, 2007
Electrochemical Analysis of Potentials and Nucleation Mechanism for (Tl0.8Pb0.2Bi0.2) (Sr0.9Ba0.1)2 Ca2.2Cu3Ox Films in Dimethyl Sulfoxide (DMSO)
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The basic electrodeposition characteristics for the fabrication of Tl, Pb, Bi, Sr, Ba, Ca, Cu (Tl-1223) precursor films in dimethyl sulfoxide (DMSO) were investigated by using the electrochemical method as a cathodic polarization and a chronamperometric technique. Potential differences of ca. -0.2 V were observed in non-aqueous solution, compared with the electromotive force (EMF) series calculated from an aqueous solution. The deposition behavior was divided into two groups [Tl, Pb, Bi, Cu (TPBC) and Sr, Ba, Ca (SBC)], to investigate the morphologies and nucleation mechanisms suggested by the Scharifker and Hills model. The nucleation mechanism of Tl deviated from the instantaneous and progressive curves, depositing dendrite deposits, while Sr fit the instantaneous curve, depositing hemispherical and spherical geometries; the amount of material deposited was influenced by the deposition time. At the early stage, Sr compressed the growth of Tldeposited dendrite shapes, showing a low Tl:Sr ratio. After 200 s, the Tl:Sr ratio also decreased, creating a new nucleation growth on the deposited particles, which increased the growth rate of the powdery layer while the compact layer was decreasing. Four desired stoichiometric precursor films were obtained in the sequence of one batch of eletrolyte, depositing the seven elements at almost the same growth rates as the time increased.
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