Underachieved capacity and low voltage plateau is ubiquitous in conventional aqueous magnesium ion full batteries.S uch limitations originate from the electrochemistry and the lowc arrier-hosting ((de)intercalation) potential of electrode materials.H erein, via as trategy of enhancing the electrochemistry through carrier-hosting potential compensation, high-energy Mg 2+ /Na + hybrid batteries are achieved. A Mg 1.5 VCr(PO 4) 3 (MVCP) cathode is coupled with FeVO 4 (FVO) anode in an ew aqueous/organic hybrid electrolyte, giving reliable high-voltage operation. This operation enables more sufficient (de)intercalation of hybrid carriers (Mg 2+ / Na +), therebye nhancing the reversible capacity remarkably (233.4 mA hg À1 at 0.5 Ag À1 ,92.7 Wh kg À1 electrode ,that is, ! 1.75fold higher than those in conventional aqueous electrolytes). The relatively high Na +-hosting potential of the electrodes compensates for the lowM g 2+-hosting potential and widens/ elevates the dischargep lateau of the full battery up to 1.50 V. Mechanism study further reveals an unusual phase transformation of FVOt oF e 2 V 3 and the low-lattice-strain pseudocapacitive (de)intercalation chemistry of MVCP.