“…Thus far, the effective regulation routes lie predominantly in the following aspects: (i) insulation of the metallic Na from severe electrolyte corrosion by constructing ionic-conductive protective coating on the deposition substrates, such as polymer brush macromolecules (polyether amine ''PEA''), porous ceramics (Al 2 O 3 , aluminum alkoxide ''alucone''), or carbonaceous over-coating intermediates (hollow carbon spheres and multilayer graphene). 20,[31][32][33][34][35][36][37][38] Although the homogenized Na + flux toward the substrate was achieved, these methods neglected the manipulation at the nucleation stage, resulting in dendrite formation upon high-capacityloadings; (ii) designing the sodiophilic architectures, for instance, the Na 15 Sn 4 host, ZnO/carbon fiber network, or Ag nanowires, etc., with a high surface area and reduced local current density to stagnate the nucleation. [39][40][41][42] Nonetheless, the large mass/volume portion of the metallic substrate in the cell models would come at the expense of theoretical energy density.…”