Enhancing the cycle stability of milled Mg-Ni alloys: The role of Pd substitution on reversible electrochemical hydrogenation/dehydrogenation reactions

• Pd addition enables reversible electrochemical hydrogenation/dehydrogenation reactions in the Mg 2 Ni phase. • Pd addition enhances the electrochemical reaction kinetics of milled Mg-Ni alloys. • Pd addition improves both cyclic performance and rate capability of milled Mg-Ni alloy anodes. • The result of this work provides a deeper understanding on electrochemical hydrogen storage performances of Mg-based alloys. The practical application of Mg-based alloys as anode materials for nickel-metal hydride (Ni-MH) batteries is hindered by serious capacity decay. To enhance their cycle stability and elucidate the underlying mechanism, this study investigates the influence of partially substituting Ni with Pd on the structural and electrochemical properties of milled Mg 55 Ni 45 alloy, as well as their microstructural evolution during cycling. This work demonstrates the Pd addition enables reversible electrochemical hydrogenation/dehydrogenation reactions in the Mg 2 Ni phase and enhances the electrochemical reaction kinetics of the alloys. As a result, the addition of Pd improves both cyclic performance and rate capability of the milled alloy electrodes. The Mg 55 Ni 45 alloy delivers a maximum discharge capacity of 488.65 mAh/g but decays to 110 mAh/g after only 13 cycles at a discharge current density of 50 mA/g. In contrast, the Mg 55 Pd 4 Ni 41 alloy demonstrates a discharge capacity of 564.6 mAh/g and retains 277 mAh/g after 50 cycles. Notably, when subjected to a higher discharge current density of 300 mA/g, the Mg 55 Pd 4 Ni 41 alloy displays an enhanced discharge capacity (401.49 mAh/g) compared to that of the Mg 55 Ni 45 alloy (77.72 mAh/g).