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NanotechNewsLithiated PAA‐Coated SiOx Anode for Stable and High‐Capacity Lithium‐Ion Batteries: Interfacial Regulation and Volume Expansion Suppression
Lithiated PAA‐Coated SiOx Anode for Stable and High‐Capacity Lithium‐Ion Batteries: Interfacial Regulation and Volume Expansion Suppression
Nanotech

Lithiated PAA‐Coated SiOx Anode for Stable and High‐Capacity Lithium‐Ion Batteries: Interfacial Regulation and Volume Expansion Suppression

•January 29, 2026
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Small (Wiley)
Small (Wiley)•Jan 29, 2026

Why It Matters

The breakthrough tackles silicon anodes' expansion and conductivity limits, unlocking higher‑energy, longer‑life lithium‑ion batteries for electric vehicles and grid storage.

Key Takeaways

  • •LiPAA coating creates conductive network
  • •Specific capacity 1234 mAh/g after 200 cycles
  • •Full cell retains 86.4% after 500 cycles
  • •LiF‑rich SEI reduces electrolyte consumption
  • •Spray‑drying enables scalable production

Pulse Analysis

Silicon‑based anodes have long been touted as the next leap in lithium‑ion energy density because silicon can store roughly ten times more lithium than graphite. However, practical deployment has been hampered by two fundamental drawbacks: massive volume expansion—up to 300 % during lithiation—and intrinsically low electronic conductivity. These issues trigger continuous electrolyte decomposition, unstable solid‑electrolyte interphase (SEI) growth, and rapid capacity fade, especially under high‑rate cycling demanded by electric‑vehicle powertrains.

The recent study introduces a lithiated polyacrylic acid (LiPAA) coating applied to micron‑sized SiOx via spray drying, forming spherical SiOx@LiPAA composites. LiPAA infiltrates the particle surface, establishing an elastic polymer matrix that buffers expansion while simultaneously creating a percolating conductive network. Moreover, the polymer promotes formation of a thin, LiF‑rich SEI that curtails parasitic reactions and stabilizes interfacial impedance. The spray‑drying route is compatible with existing roll‑to‑roll processes, suggesting a low‑cost, scalable manufacturing pathway.

Electrochemical testing shows the SiOx@LiPAA anode delivers 1 234 mAh g⁻¹ after 200 cycles at 0.5 C and retains 536 mAh g⁻¹ at a demanding 4 C rate. In a full‑cell configuration with a LiFePO₄ cathode, the system maintains 86.4 % capacity after 500 cycles, surpassing most silicon‑oxide benchmarks. Such durability and rate capability address the primary concerns of automotive battery packs, where long cycle life and fast charging are critical. If adopted, this technology could accelerate the transition to higher‑energy‑density packs without sacrificing manufacturing economics, positioning silicon‑based anodes as a viable competitor to graphite in next‑generation EVs. Industry analysts estimate that integrating such anodes could boost vehicle range by up to 15 %. Manufacturers will need to validate long‑term thermal stability under real‑world conditions.

Lithiated PAA‐Coated SiOx Anode for Stable and High‐Capacity Lithium‐Ion Batteries: Interfacial Regulation and Volume Expansion Suppression

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