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<p>Silicon-based solid-state batteries are promising next-generation high-energy-density technologies. However, poor (electro)chemical compatibility between silicon negative electrodes and solid electrolytes (e.g., Li<sub>6</sub>PS<sub>5</sub>Cl) plus sluggish interfacial kinetics severely limits their reversibility and Coulombic efficiency. Here, we propose a surface halogenation strategy that transforms the native amorphous SiO<sub>2</sub> passivation layer on silicon particles into a functional Al(Si)OCl composite surface via controlled reaction with AlCl<sub>3</sub>. This artificial interphase reconciles interfacial incompatibility and enables fast ionic/electronic transport, suppressing irreversible lithium loss. The optimized negative electrode achieves a high initial Coulombic efficiency of 94.3% in half-cells and 85.6% initial Coulombic efficiency (86.6% with pre-lithiation) in full cells paired with LiNi<sub>0.88</sub>Co<sub>0.09</sub>Mn<sub>0.03</sub>O<sub>2</sub>. Enhanced reversibility further delivers long-term cyclability. The optimized negative electrode delivers 86% capacity retention and 99.998% average Coulombic efficiency over 200 cycles. Even at high-loading ( &gt; 10 mAh cm<sup>-2</sup>, and no adhesives/conductive carbon/electrolyte), it retains 72% capacity after 500 cycles. The full cells maintain 80% capacity after 200 cycles at 1 C, with an average Coulombic efficiency exceeding 99.95%. The versatility of this halogenation strategy underscores halide chemistry’s broad potential in advancing high-performance, reversible silicon-based solid-state batteries.</p>

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Surface halogenation engineering for reversible silicon-based solid-state batteries

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年12月27日

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  • Haosheng Li,
  • Yaru Li,
  • Guantai Hu,
  • Ying Li,
  • Caijin Xiao,
  • Liang Zhao,
  • Huiqin Huang,
  • Haochang Zhang,
  • Wei Xia,
  • Ning Lin

摘要

Silicon-based solid-state batteries are promising next-generation high-energy-density technologies. However, poor (electro)chemical compatibility between silicon negative electrodes and solid electrolytes (e.g., Li6PS5Cl) plus sluggish interfacial kinetics severely limits their reversibility and Coulombic efficiency. Here, we propose a surface halogenation strategy that transforms the native amorphous SiO2 passivation layer on silicon particles into a functional Al(Si)OCl composite surface via controlled reaction with AlCl3. This artificial interphase reconciles interfacial incompatibility and enables fast ionic/electronic transport, suppressing irreversible lithium loss. The optimized negative electrode achieves a high initial Coulombic efficiency of 94.3% in half-cells and 85.6% initial Coulombic efficiency (86.6% with pre-lithiation) in full cells paired with LiNi0.88Co0.09Mn0.03O2. Enhanced reversibility further delivers long-term cyclability. The optimized negative electrode delivers 86% capacity retention and 99.998% average Coulombic efficiency over 200 cycles. Even at high-loading ( > 10 mAh cm-2, and no adhesives/conductive carbon/electrolyte), it retains 72% capacity after 500 cycles. The full cells maintain 80% capacity after 200 cycles at 1 C, with an average Coulombic efficiency exceeding 99.95%. The versatility of this halogenation strategy underscores halide chemistry’s broad potential in advancing high-performance, reversible silicon-based solid-state batteries.