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We report a porous Na–Si framework (NaSi4) identified via a Na-templated crystal structure search, which integrates nontrivial topological electronic states with high-performance sodium-ion storage. NaSi4 crystallizes in an orthorhombic architecture consisting of interpenetrating sp3-bonded silicon frameworks that form one-dimensional Na-filled channels. Upon Na removal, the resulting silicon host (Si16) preserves the open-channel topology and structural integrity. Electronic structure calculations reveal symmetry-protected band crossings near the Fermi level, establishing Si16 as a topological nodal-line semimetal with intrinsically robust electronic conductivity. Benefiting from the built-in conductivity and accessible diffusion channels, the Si16 framework delivers a high reversible Na-storage capacity of ~ 239 mAh·g−1 at an average insertion voltage of ~ 0.52 V (vs. Na/Na+). First-principles calculations further indicate strong Na binding, fast one-dimensional Na+ migration, and excellent structural stability. This work demonstrates a viable Na-templated design strategy for multifunctional silicon anodes and highlights the potential of coupling topological electronic states with energy-storage materials.

This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (CC BY 4.0, https://creativecommons.org/licenses/by/4.0/).
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