Synthesis and hydrogenation properties of Ni–Co bimetallic nanoparticles

The kinetics of the formation of bimetallic Ni–Co nanoparticles (Ni–Co-NPs) via the reduction of Ni and Co hydroxides by hydrazine in alkaline water/ethylene glycol solution has been studied. It was found that the rate of the Ni–Co-NPs nucleation linearly depends on the initial concentration of Ni(OH) 2 . However, the rate of nanoparticles growth is sharply increased in the case of bimetallic Ni–Co-NPs compared to Ni-NPs and almost does not change over the entire range of Ni/Co ratio. Using the scanning electron microscopy (SEM) and the X-ray diffraction analysis, it was found that the mean size and the polydispersity of Ni–Co-NPs are decreased with the decrease of the fraction of Ni up to 50% but are increased in the case of Ni 25 Co 75 . The electrochemical charge/discharge multicycling of NPs electrodes was carried out in view of material potential usefulness as conductive metallic binder with own capacity for Ni/MH batteries. Replacing the Ni by Co in Ni–Co-NPs increases the discharge capacity of the electrode to 63 mAh/g for the Ni 50 Co 50 composition. Cyclic stability of Co-free NPs is visibly better in comparison with binary Ni–Co-NPs. Additional electrochemical measurements for the Ni-NPs and Ni 50 Co 50 -NPs showed that the high rate dischargeability, HRD 1000 , is increased from 54 to 74%, but the discharge time according to the chronoamperometric data drastically is decreased at constant potential of − 0.6 V vs Ag/AgCl electrode.