Abstract
Solid-state lithium metal batteries face challenges from irreversible interfacial degradation and sluggish ion transport. We propose an electron-funnel-mediated anion confinement strategy via atomic-level electronic field engineering. Incorporating electron-withdrawing –NO2 groups into Zr-based frameworks induces a 0.38 eV upward d-band center shift, generating a quantum-confined electrostatic gradient that polarizes TFSI− anions. This reduces TFSI− decomposition energy barrier (ΔG: −0.35 → −1.22 eV), selectively promoting LiF nucleation while suppressing side reactions. Concurrently, Zr4+-PEO Lewis interactions disrupt polymer crystallinity, enhancing ionic conductivity and Li+ transference number. Cryo-TEM tomography and TOF-SIMS mapping reveal a fractal LiF-rich interphase enabling dendrite-free lithium plating for > 11,000 h with polarization < 40 mV. LiFePO4 full cells achieve 86.3% capacity retention after 400 cycles at 1C (1.3 mAh cm−2). This work establishes anion confinement as a universal framework synchronizing ion transport and interfacial durability, advancing practical solid-state batteries with exceptional longevity.
| Original language | English |
|---|---|
| Article number | 100452 |
| Journal | eScience |
| Volume | 6 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - Jan 2026 |
Keywords
- Electron-funnel engineering
- Ionic transport
- Robust interface
- Solid-state lithium metal battery
- Solid-state polymer electrolytes