Electrochemical preparation La–Co magnetic alloy films from dimethylsulfoxide

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Abstract

The electrochemical behavior of La3+ ion is investigated on a Pt electrode in the 2.5 × 10−3 mol L−1 La(ClO4)3–7.5 × 10−2 mol L−1 LiClO4–dimethylsulfoxide (DMSO) system. The experimental results indicate that the reduction of La3+ ion is irreversible. Some electrochemical parameters are measured. The pulse deposition technique is used to prepare La–Co alloy films. The surfaces of La–Co alloy films are uniform, compact and showed a metallic luster. The grain sizes of La–Co alloy observed by scanning electron microscope (SEM) are about 100 nm. La–Co alloy film is amorphous as proven by the X-ray diffraction (XRD). The magnetic properties of the amorphous La–Co alloy film are measured.

Introduction

Rare earths and their alloys exhibit interesting magnetic, optical, electric, and hydrogen storage properties, that have been widely applied to the development of various functional materials [1], [2], [3]. La–Co alloys possess magnetic properties. The main interest of the study is focused on magnetic properties associated with the interfacial spin polarization induced in a 3d transition metal (TM) by a rare earth (RE) element via the 4f–3d interaction, through the 5d–3d hybridisation. The thin-film structures have been found useful in a wide range of applications in a few years. The properties of low-dimensional layered structures are quite different from those found previously in bulk materials [1]. La–Co alloy films have mainly been prepared through physical methods [4], [5]. Since rare earth elements are very active, it is very difficult to deposit them from aqueous solution using electrochemical methods. Recently, we have studied the electrodeposition of rare earths and their alloys from organic solutions at room temperature [6], [7]. In this paper, the kinetic parameters of La3+ ion are measured and La–Co alloy films are prepared by pulse electrodeposition in dimethylsulfoxide (DMSO).

Section snippets

Experimental

The LaX3·6H2O obtained by the reaction of La2O3 (99.95%) and HNO3 (AR), HCl (AR) and HClO4 (AR) were dehydrated in vacuum at 353 K. LiClO4 (AR) was dehydrated in vacuum at 453 K. The dimethylsulfoxide was dehydrated with 4 Å molecular sieves and distilled to remove impurities at reduced pressure.

The conductivity of LaX3 (X = NO3, Cl and ClO4)was measured by DJS-12 data conductivitimeter in DMSO. The temperature was controlled at 298 K. A tri-electrode cell was used as the electrochemical measurement

The conductivity of lanthanum salts in dimethylsulfoxide

Dimethylsulfoxide is a fine, non-proton polar solvent. Lanthanum salts are highly soluble in dimethylsulfoxide. The conductivity of LaX3 (X = NO3, Cl and ClO4) is measured in DMSO at 298 K. The molar conductivity Λm is expressed asΛm=κcwhere κ and c are the conductivity and concentration of lanthanum salts, respectively. The plot of Λmc of three lanthanum salts in DMSO is shown in Fig. 1. According to Kohlrausch experiential regulation [8], Λm and c are following, as this equation when the strong

Conclusion

Dimethylsulfoxide (DMSO) is a fine, non-proton polar solvent. La(ClO4)3 has strong electrolyte property in DMSO. Its limiting molar conductivity Λm is 1.56 × 102 S cm2 mol−1. La(ClO4)3 also has highly soluble in DMSO. Thus, La(ClO4)3 is used as the research salt in the electrodeposition system. The electrochemical behavior of La3+ ion is studied on a Pt electrode in the 2.5 × 10−3 mol L−1 La(ClO4)3–7.5 × 10−2 mol L−1 LiClO4–DMSO system at 300 K. The experimental results indicated that the reduction of La3+

Acknowledgements

This research was financially supported by the Natural Science Foundation, Project No. 04300695 and the Science and Technology Project, Project No. 2KM02304G, Guangdong Province, PR China.

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