Surface-Confined Lithium Plating Enabled by Externally Anchored MgF<sub>2</sub> Nanodots on Hollow Carbon Spheres for Dendrite-free Anodes.
basic_science · Level V
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- Record sourced from PubMed, PMID 41930624.
- Also identified by DOI 10.1021/acsnano.6c00616.
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Abstract
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<sub>2</sub>) 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<sub>2</sub> nanodots are uniformly anchored exclusively on the external surface of <i>N</i>-doped hollow carbon spheres (MgF<sub>2</sub>/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<sub>3</sub>N. Consequently, the MgF<sub>2</sub>/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<sub>4</sub>. This work demonstrates the effectiveness of an external-modification paradigm, offering a scalable alternative to intricate internal designs for stabilizing lithium-metal batteries.