Orthorhombic V 2 O 5 is a promising Mg battery cathode material, and reversible intercalation in the layered α-phase has been claimed experimentally. However, these results, based on electrochemistry and XRD, are controversial. Previous computational studies have predicted high activation barriers (∼1 eV) for ionic migration in α-V 2 O 5 , although improved Mg 2+ mobility is expected in the δ -phase. Here, hybrid-exchange density functional theory is used to discuss structure, stability and intercalation in the α and δ phases, beginning with a model system with MV 2 O 5 stoichiometry, and varying ionic radius of the M cations. The relative stability of the two phases upon intercalation of M is rationalised through a tolerance factor-like behavioural trend, providing a framework for phase selection using intercalants of different ionic size. This tolerance factor behaviour is due to the presence of ferroelectrically distorted (2×2×2) perovskite blocks within the α-V 2 O 5 structure. The δ -phase is found to undergo a barrierless phase change to α in fully charged (de-intercalated) Mg x V 2 O 5 (x=0), indicating that stabilisation of δ -Mg x V 2 O 5 is required at low x if the δ phase is to be retained for higher Mg mobility. By employing dispersion interactions to accurately reproduce the interlayer distance, activation barriers for ion migration are found to be higher than reported in previous studies, clarifying questions regarding the extent of Mg intercalation that can be achieved experimentally. Interlayer ions are found to lower activation barriers for Mg 2+ mobility by up to ∼330 meV in the α phase by expanding the interlayer space. The results address open questions about the electrochemical performance of orthorhombic V 2 O 5 as Mg battery cathode material, and indicate atomic level mechanisms that activate ionic mobility in layered V 2 O 5 .One fundamental route to improving energy density is to move from sulphide to oxide based materials which have higher ionic character, thus providing higher voltages vs. Mg metal, whilst the lower atomic mass of O relative to S reduces weight. 7 However the very feature that enhances intercalation voltage, i.e. the stronger electrostatic interaction between the Mg ion and the anionic framework of the oxide cathode host, also increases acti-J o u r n a l N a me , [ y e a r ] , [ v o l . ] , 1-13 | 1 2 | 1-13 J o u r n a l N a me , [ y e a r ] , [ v o l . ] ,