This paper describes the hydrogen storage properties of Magnesium rich ternary Mg-Ni-Cu films of 1.5 mu m thickness using binary Mg-Ni and Mg-Cu as baselines, and aims to elucidate the precise influences of alloying element Cu on the hydrogen sorption kinetics, thermodynamics and cycleability. Mg-rich Mg-Ni-(Cu) alloys show two stages during absorption. The first stage due to the absorption of Mg not alloyed in the form of Mg(2)Ni and Mg(2)Cu, hereafter denoted as free-Mg, is very quick, but the second one due to the absorption of intermetallic Mg(2)Ni and/or Mg(2)Cu is significantly slower. This sequence is confirmed by XRD characterizations at different absorption stages. The rapid first stage absorption is mainly catalyzed by the intermetallic phase, Mg(2)Ni. Cu substitution improves the desorption kinetics, but severely decreases the kinetics of the second absorption stage. Failure to completely absorb Mg(2)Cu to MgH(2) and MgCu(2) in consecutive absorption cycles leads to complete loss of desorption-ability in binary Mg-15 at.%Cu. XRD combined with TEM shows that segregation of Mg(2)Cu towards the grain boundaries is responsible for this. Pressure-Composition Isotherms are used to examine the thermodynamic properties of the alloys. The thermodynamic properties of the Low-Temperature (LT-) Mg(2)NiH(4) are determined for the first time experimentally, and are found to be Delta H = 78.6 kJ/mol H(2) and Delta S = -147.83 J/K-mol H(2). It is found that the Cu substitution has no influence on the plateau pressure of MgH(2) from free-Mg phase, but slightly increases the plateau pressure of LT-Mg(2)NiH(4). (C) 2010 Professor T. Nejat Veziroglu. Published by Elsevier Ltd. All rights reserved.