“…Rechargeable magnesium batteries (RMBs) based on Mg anodes have been considered as one of the potential alternatives to secondary batteries due to their high theoretical volumetric specific capacity (3833 mA h mL –3 ), rich natural abundance, low price, and dendrite-free deposition process. , However, RMBs still have no satisfactory practical application owing to several obstacles. First, highly polarized divalent Mg 2+ ions have strong Coulombic interactions with cathode materials, which usually leads to sluggish diffusion/insertion kinetics within the crystal lattices of cathode. − In addition, only a few electrolytes can meet high Coulombic efficiency for Mg plating/stripping and satisfying compatibility with existing electrode materials. − Therefore, the development of cathode materials capable to reversibly Mg 2+ storage with high capacity, fast kinetics, and outstanding cycling stability is still a great challenge. − Aurbach’s group first constructed the RMBs using Chevrel phase Mo 6 S 8 as top-performing cathode material in 2000, a milestone development in the field of RMBs. Although Chevrels are considerable for RMBs, their theory discharge capacity (128.8 mA h g –1 ) and low intercalation voltage (1.1 V vs Mg 2+ /Mg) drastically limit their energy density. , Subsequently, only a few cathode materials with gratifying capacity and cycling stability for RMBs have been developed, including transition metal oxides (V 2 O 5 , MnO 2 ), − olivine-phase MgFeSiO 4 , and layered transition-metal chalcogenides (TMCs, MoS 2 , TiS 2 , and WSe 2 ). − Among them, the metal oxides and polyanionic olivine are faced with sluggish kinetics and shaky cycling stability. , In comparison, TMCs exhibit enhanced mobility of Mg 2+ ions , owing to the weaker Coulombic attraction between the “soft” anionic lattices (S or Se) and guest Mg 2+ ions. − …”