Synergistic Coupling of Host and Electrolyte Achieving 1270 Wh L<sup>-1</sup> in Anode-Free Lithium Metal Batteries.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 41178147.
- Also identified by DOI 10.1002/adma.202515906 and PMC identifier 12966975.
- Licence recorded as CC BY-NC.
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Abstract
Anode-free lithium metal batteries (LMBs) represent a promising avenue for maximizing energy density by eliminating excess lithium (Li), yet their practical implementation is impeded by limited Li reversibility and pronounced interfacial instability. Herein, a synergistic coupling strategy is reported that integrates a highly reversible host (RH) with a rationally designed, carbonate-rich electrolyte (DEL) to concurrently address these fundamental challenges. The RH spontaneously induces the formation of a robust Li<sub>2</sub>O- and Li<sub>3</sub>N-rich solid electrolyte interphase via electron transfer, which effectively accommodates Li volume changes and suppresses dendritic growth. Complementarily, DEL, composed of commercially available salts, solvents, and additives, establishes stable electrode-electrolyte interphases at both electrodes. Coin-type anode-free full cells employing the RH-DEL configuration achieve an average Coulombic efficiency of 99.6% and 81.9% capacity retention after 100 cycles at 4.6 mAh cm<sup>-2</sup> and 2.3 mA cm<sup>-2</sup>. Stacked pouch-type full cells further deliver a record volumetric energy density of 1270 Wh L<sup>-1</sup> (including packaging) under lean electrolyte (E/C = 2.5 g Ah<sup>-1</sup>) and a low stack pressure (≈20 kPa). This synergistic approach delineates a practical pathway toward high-energy, long-life anode-free LMBs for advanced energy storage systems.