Article ID Journal Published Year Pages File Type
1258750 Journal of Rare Earths 2013 9 Pages PDF
Abstract

The La0.5Pr0.2Zr0.1Mg0.2Ni2.75Co0.45Fe0.1Al0.2 (M1) and Zr0.65Ti0.35(Mn0.2V0.2Cr0.15Ni0.45)1.76 (M2) hydrogen storage alloys were prepared by inductive melting. In addition, the M1+30 wt.%M2 composites were successively prepared by using high-energy ball milling technology. From the X-ray diffraction (XRD) analysis, it was found that M1 and M2 alloys still retained their respective main phases in the M1+30 wt.%M2 composites. The scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS) indicated that the decrease in discharge capacity of M1 and M2 alloy electrodes was ascribed to the oxidation-dissolution of La, Pr, Mg and Ti, Mn, V, Cr active elements, respectively. The electrochemical studies showed that the M1+30 wt.%M2 composite electrode ball milling for 5 min exhibited excellence cyclic stability (92.3%) after 80 charge/discharge cycles, which was higher than 77.7 % and 85.6% of M1 and M2 alloy electrodes, respectively. Moreover, at the discharge current density of 1200 mA/g, the high rate discharge ability (HRD) of the M1+30 wt.%M2 composite electrode increased from 61.5% (5 min) to 70.3% (10 min). According to the linear polarization, Tafel polarization and cyclic voltammograms (CV), the electrochemical kinetics of hydrogen reaction on the surface of the electrode and hydrogen diffusion rate in the bulk of alloy were also improved in the M1+30 wt.%M2 composite with increasing ball milling time.

Graphical AbstractCharge/discharge cycle life of M1, M2, M3 and M4 alloy electrodes at 303 K, respectivelyFigure optionsDownload full-size imageDownload as PowerPoint slide

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Physical Sciences and Engineering Chemistry Chemistry (General)
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