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The present work is focused on the studies of the phase-structural transformations in the La3-xMgxNi9 (x ​= ​1.0, 1.1 and 1.2) alloys as active materials of negative electrodes in the Nickel-Metal Hydride (Ni/MH) batteries. The phase equilibria and phase-structural transformations in the alloys were probed by in situ neutron powder diffraction (NPD) at the temperatures ranging from 300 ​K to 1273 ​K using the measurements of the equilibrated alloys at 8 setpoint temperatures of 300, 973, 1073, 1123, 1173, 1223, 1248 and 1273 ​K. Prepared by induction melting initial alloys were found to be multi-phase structured, containing up to 6 individual intermetallic compounds with different stoichiometric compositions. With the increase of the temperature and holding time, various transformations took place in the studied alloys. These included the formations and transformations of super-stacking intermetallics with variable ratios (La ​+ ​Mg)/Ni, 1:3, 2:7 and 5:19. With increasing temperatures, several systematic changes took place. (a) Abundances of (La,Mg)2Ni4 AB2 and (La,Mg)Ni3 AB3 type intermetallics gradually decreased before they melted/decomposed above 1073 ​K; (b) The (La,Mg)2Ni7 A2B7 type intermetallics began to decrease in abundances above 1123 ​K; (c) The transformation in the (La,Mg)5Ni19 intermetallics from 3R to 2H proceeded above 1223 ​K. The increase of Mg content had no obvious influence on (La,Mg)2Ni4 and (La,Mg)2Ni7 phases, and corresponding reactions R1 and R3 took place at the same temperatures as in the La–Ni system. However, with increasing Mg content the melting point of (La,Mg)5Ni19 phase increased while the melting point of the (La,Mg)Ni3 phase it decreased, leading to the variation of the reaction temperatures of the corresponding processes. The present study will assist in optimizing phase-structural composition of the alloys in the La–Mg–Ni system which contain Mg-modified layered structures by tailoring the high temperature annealing conditions.

The effect of Mo-addition on hydrogen storage and low-temperature electrochemical performances of La-Mg-Ni-Co-Al alloys is investigated. The alloys were synthetized via vacuum induction melting followed by annealing treatment at 1123 K for 8 h. The major phases in the annealed alloys are consisted of (La, Mg) 2 Ni 7 , (La, Mg) 5 Ni 19 and LaNi 5 phases. Mo-addition facilitates phase transformation of LaNi 5 into (La, Mg) 2 Ni 7 and (La, Mg) 5 Ni 19 phases. Hydrogen absorption/desorption PCI curves indicates that the hydrogen storage capacity of the alloy increases remarkably with the addition of Mo. Furthermore, the La 0.75 Mg 0.25 Ni 3.05 Co 0.2 Al 0.05 Mo 0.2 alloy shows excellent hydriding/dehydriding kinetics with a higher capacity, requiring only 100 s to reach its saturated hydrogen capacity of 1.58 wt% at low temperature of 303 K, and releasing 1.57 wt% hydrogen within 400 s at 338 K. Electrochemical experiments manifest that the Mo-added alloy electrode has perfect activation properties and the maximum discharge capacity. The low-temperature dischargeability shows that the La 0.75 Mg 0.25 Ni 3.05 Co 0.2 Al 0.05 Mo 0.2 alloy exhibits the excellent low-temperature discharge performance, and the maximum discharge capacity is improved from 231.0 to 334.6 mAh/g at 253 K. The HRD property of the alloy electrode is enhanced, suggesting that Mo enhances the kinetic ability at low-temperature.