Electrochemistry of Zn(II)/Zn on Mg alloy from the N-butyl-N-methylpyrrolidinium dicyanamide ionic liquid

被引:62
|
作者
Deng, Ming-Jay [1 ]
Lin, Pei-Chiung [2 ]
Chang, Jeng-Kuei [3 ]
Chen, Jin-Ming [1 ]
Lu, Kueih-Tzu [1 ]
机构
[1] Natl Synchrotron Radiat Res Ctr, Hsinchu, Taiwan
[2] Natl Cheng Kung Univ, Dept Chem, Tainan 70101, Taiwan
[3] Natl Cent Univ, Inst Mat Sci & Engn, Tao Yuan, Taiwan
关键词
Electrodeposition; Ionic liquid; AZ91D; Zn; Corrosion; Dicyanamide; MAGNESIUM ALLOY; CORROSION BEHAVIOR; MOLTEN-SALT; ELECTRODEPOSITION; CHLORIDE; ZINC; ALUMINUM; METALS; AIR; TIN;
D O I
10.1016/j.electacta.2011.04.082
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Electrochemical reaction of Zn(II)/Zn on glassy carbon electrode(GC) and Mg alloy substrates was investigated in the room-temperature ionic liquid, N-butyl-N-methyl-pyrrolidinium dicyanamide (BMP-DCA) containing ZnCl2 at 323 K. Amperometric titration experiments suggest that Zn(II) reacted with DCA anions forming [Zn(DCA)(3)](-) complex anion, which also could be reduced to Zn metal via a single-step electron transfer process. By chronoamperometric measurements, the electrodeposition of Zn on GC and Mg alloy substrates involved three-dimensional instantaneous nucleation under diffusion control at 323 K. The Zn deposits are also systematically characterized by the techniques of powder X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The Zn layer deposited at a lower current density on Mg alloy substrates was more compact and uniform when compared to that deposited at a higher current density: consequently, this coating revealed a protection capability for the Mg substrate against corrosion. (C) 2011 Elsevier Ltd. All rights reserved.
引用
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页码:6071 / 6077
页数:7
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