10 À4 % of Li. The ionic radii of Mg 2þ , 0.86 Å, and Li þ , 0.90 Å, are rather similar, [1] but Mg has the advantage of being a bivalent ion, which leads to a higher volumetric capacity of Mg metal anodes compared to Li, 3833 mAh cm À3 versus 2062 mAh cm À3 , and also to a low reduction potential of À2.37 V versus the standard hydrogen electrode (SHE) compared to À3.05 V of Li. [9,10] Furthermore, Mg-ion batteries (MIBs) exhibit a low tendency for dendrite formation [11][12][13][14][15] and a high melting point.A high multivalent ionic conductivity of 1-10 mS cm À1 has been achieved in MIBs at high temperatures. [16,17] However, a major problem for MIBs lies in the sluggish kinetics during intercalation at room temperature. [2,18] It should be noted that the design of chemically stable electrodes with high ionic conductivity is highly desirable, [2,[19][20][21][22][23] as a low ionic mobility can severely limit the performance of batteries.To address the slow migration of Mg ions in cathode materials at low temperatures, Chevrel phases and layered and spinel TiS 2 structures have been studied in detail. [24] A Mg-ion migration barrier of about 550 meV was found in cubic Ti 2 S 4 using galvanostatic intermittent titration technique measurements. Note that typically maximum migration barriers of %525 meV for micron-sized particles and %650 meV for nanosized particles are assumed to be compatible with an adequate battery operation. [25] Studies on the sulfide and selenide spinel frameworks indicate low-energy barriers for Mgion diffusion comparable to those of LIBs. [26] In contrast, oxide spinel cathode materials exhibit high migration barriers for Mg ions, which are caused by the relatively strong Coulombic attraction between the guest Mg 2þ and host oxygen lattice, [23] which leads to a lower ion mobility. The smaller electronegativity of sulfur and selenium lattices enlarges the lattice constant of these materials and thus also their ion mobility as typically diffusion barriers become smaller for larger lattice constants. Nevertheless, the increase of the ion mobility through the lowering of diffusion barriers is also accompanied by lower Mg insertion energies into the spinel structures, which lowers the voltage [27,28] and thus causes a reduction of the energy densities of chalcogenide materials.Recently, MgSc 2 Se 4 has been found to be a super ionic conductor exhibiting a high Mg-ion conductivity of 0.1 mS cm À1 at room temperature. [26] This high ion mobility not only makes MgSc 2 Se 4 a promising cathode material for MIBs, but also suggests that it could be used as a solid electrolyte. However, solid