Penghao Song, Dongdong Li, Yanan Sun, Xin Peng, Xiaohan Wang, Xinfeng Li, Shengchen Yang, Wen‐Yong Lai
The advancement of lithium–metal anodes is critically hampered by uncontrollable lithium deposition, especially on lithiophobic three-dimensional carbon hosts where surface plating negates their structural benefits. While internal modification with lithiophilic agents (e.g., MgF 2 ) is a common strategy, it often suffers from synthetic complexity and nanoparticle agglomeration, leading to inconsistent performance. Herein, we propose a strategic shift in host architecture by designing a composite where ultrafine MgF 2 nanodots are uniformly anchored exclusively on the external surface of N -doped hollow carbon spheres (MgF 2 /NHCS). This precise external engineering, achieved via a controlled in situ conversion process, effectively prevents agglomeration and creates a continuous, homogeneous network of nucleation sites. This design enforces a conformal lithium-plating front, guiding the formation of a dense, spherical metallic layer that encapsulates the host. Concurrently, it synergistically fosters a highly robust, inorganic-rich solid–electrolyte interphase composed of LiF and Li 3 N. Consequently, the MgF 2 /NHCS host enables exceptionally stable, dendrite-free cycling over 1300 h in symmetric cells and delivers outstanding rate capability and longevity in full cells paired with LiFePO 4 . This work demonstrates the effectiveness of an external-modification paradigm, offering a scalable alternative to intricate internal designs for stabilizing lithium–metal batteries.