Abstract
High–capacity silicon oxide (SiOx)–based anodes show great potential for lithium–ion batteries (LiBs) due to their superior theoretical capacity. However, their practical application is hindered because of their severe volume expansion, poor electrical conductivity, and unstable solid–electrolyte interphase (SEI). Herein, we present a novel flexible anode architecture, where a thin–film amorphous SiOx layer is uniformly deposited between ultralight, free–standing carbon nanofiber mats and a carbon encapsulation layer, forming a robust C–SiOx–C sandwich structure. The optimized C–SiOx–C composite demonstrates exceptional electrochemical performance, including outstanding cycling stability (specific capacity of 1120 mAh g−1, capacity retention of ∼88.8% over 300 cycles at 0.2 A g−1), enhanced rate capability, and markedly reduced SEI resistance compared with uncoated SiOx–C. Electrochemical impedance spectroscopy and galvanostatic intermittent titration reveal that the carbon coating effectively enhances electronic conductivity, stabilizes the SEI, and promotes lithium–ion diffusion kinetics (9.83 × 10 cm2 s−1). Furthermore, full–cell tests of our SiOx anode paired with a thin–film NCM622 cathode exhibits stable cycling for over 400 cycles, affirming its potential for next–generation, fast–charging, and high–energy–density LiBs systems.
| Original language | English |
|---|---|
| Article number | 173874 |
| Journal | Chemical Engineering Journal |
| Volume | 531 |
| DOIs | |
| State | Published - 1 Mar 2026 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- Anodes
- Carbon nanofibers
- Chemical vapor deposition
- Radio frequency magnetron sputtering
- Silicon oxides
- Thin films
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