Abstract
Hard carbon (HC) stands out as a competitive anode for sodium-ion batteries, combining abundant, sustainable precursors with desirable electrochemical properties. By employing a simple solution-based approach to control cellulose decomposition, we engineer curved pseudographitic domains with expanded interlayer spacing and rich closed pores from peanut shell precursors. The resulting PSHC-7 delivers 401 mAh g–1 at 0.06 A g–1, an initial Coulombic efficiency of 88.6%, 289 mAh g–1 at 3.0 A g–1, and 93.1% capacity retention over 4500 cycles. In situ Raman and in situ XRD reveal a multistep “adsorption–intercalation–pore filling” mechanism, while theoretical calculations confirm that hierarchical pores and pseudocapacitive effects enhance Na+ transport and storage. The full cells (NVP//PSHC-7) demonstrate practical applicability. This work provides an integrated experimental and theoretical framework linking precursor chemistry, microstructure, and electrochemical performance, offering a facile route to high-efficiency, durable, and cost-effective SIB anodes.
| Original language | English |
|---|---|
| Pages (from-to) | 2580-2589 |
| Number of pages | 10 |
| Journal | Nano Letters |
| Volume | 26 |
| Issue number | 7 |
| DOIs | |
| State | Published - 25 Feb 2026 |
Keywords
- hard carbons
- plateau capacity
- sodium storage kinetics
- sodium-ion batteries
- structural regulation
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