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

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.

► Electrodeposition of Zn was successfully demonstrnated in the water- and air-stable BMP-DCA ionic liquid. While ZnCl2 is insoluble in the BMP-TFSI ionic liquid, it dissolves easily in the BMP-DCA. ► Amperometric titration experiments indicated that Zn(II) probably complexed as [Zn(DCA)3]- with DCA- anion. ► Chronoamperometric experiments showed that the electrodeposition of Zn on GC and Mg alloy substrates involved 3D-instantaneous nucleation/growth process. ► A lower deposition rate would bring out a more uniform and compact Zn coating layer (which is also thicker) and, consequently, this coating revealed a protection capability for the Mg substrate against corrosion.