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Optimizing lithium nucleation overpotential in anode‐free garnet‐based hybrid solid‐state batteries

  • Subhajit Sarkar
  • , Joshua Budde
  • , Ingo Bardenhagen
  • , Julian Schwenzel
  • , Todd Sutherland
  • , Venkataraman Thangadurai*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

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 languageEnglish
Article numbere03537
JournalAdvanced Energy Materials
Volume15
Issue number47
Early online date10 Oct 2025
DOIs
Publication statusPublished - 16 Dec 2025

Keywords

  • Anode-free
  • Garnet-type solid electrolyte
  • Hybrid solid-liquid electrolyte
  • Puch cell
  • Solvation structure

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