“…The huge volume expansion results in rupture of the SEI film, leading to disrupted Na + flux in the vicinity and consequently causing uneven Na deposition and dendritic Na growth. In contrast, 3D EC scaffolds with abundant pore structure have sufficient internal space and can serve as a host to buffer the volume deformation of deposited Na during cycling. ,, Regrettably, the intrinsic “sodiophobicity” of the scaffolds results in poor Na affinity, typically manifesting a high Na nucleation barrier, which adversely affects uniform Na nucleation and deposition. − Currently, the incorporation of Na-alloying metals like Sn, Sb, and Zn into the scaffolds has been reported to significantly enhance their affinity for Na (“sodiophilicity”). ,,− Nevertheless, the composite Na/scaffold anode still demonstrates an unsatisfactory cycle life owing to the blocked ion diffusion pathways within the EC scaffolds. , Sluggish ion diffusion kinetics may lead to the preferential Na + deposition on the top surface of the scaffolds rather than being densely filled, which undermines the structural benefits of the 3D scaffolds in regulating Na nucleation and spatial confinement, a situation exacerbated at high current densities. Therefore, constructing an ideal 3D scaffold with both Na affinity and robust ion transport capabilities is crucial for achieving a highly reversible dendrite-free Na metal anode.…”