Abstract
Anode‐free solid‐state lithium batteries promise high‐energy‐density storage but remain limited by unstable interfaces between the solid electrolyte and in situ‐formed lithium. In this work, a hybrid solid–liquid electrolyte strategy is developed using a localized high‐concentration electrolyte containing AlCl3 and LiPO2F2 , a trilayer garnet‐type Li6.4Ga0.1La2.9Ba0.1Zr1.6Ta0.4O12 solid electrolyte. This configuration forms a mechanically stable and ionically conductive solid‐liquid electrolyte interphase, enabling 81% Coulombic efficiency after 300 cycles at 2 mA cm−2 and 1 mAh cm−2 in Cu/Li half‐cells. A single‐layer anode‐free hybrid solid‐state pouch cell demonstrated excellent long‐term cycling performance, retaining 75% of its initial capacity after 400 cycles at 1C (1.25 mA cm−2 ), with a Coulombic efficiency of 99% without external pressure and at room temperature. At the lab scale, this hybrid electrolyte approach shows both scalability and performance, providing a potential practical pathway to next‐generation anode‐free hybrid solid‐state lithium batteries.
| Original language | English |
|---|---|
| Article number | e03537 |
| Journal | Advanced Energy Materials |
| Volume | 15 |
| Issue number | 47 |
| Early online date | 10 Oct 2025 |
| DOIs | |
| Publication status | Published - 16 Dec 2025 |
Keywords
- Anode-free
- Garnet-type solid electrolyte
- Hybrid solid-liquid electrolyte
- Puch cell
- Solvation structure
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