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Lattice-Oxygen-Driven Selective Oxidation Strategy for Stable Argyrodite Solid-State Lithium Metal Batteries: Article No. 104986

  • Mohammad Nafis
  • , Zhiming Liang
  • , Ahmed Biby
  • , Dakota Rodriguez
  • , Ryan Tancin
  • , Donal Finegan
  • , Charles Musgrave
  • , Sehee Lee
  • , Chunmei Ban
  • University of Colorado Boulder
  • University of Utah

Research output: Contribution to journalArticlepeer-review

Abstract

All-solid-state lithium metal batteries (ASSLMBs) with Li6PS5Cl argyrodite electrolytes and high-voltage LiNi0.8Mn0.1Co0.1O2 (NMC811) cathodes offer high energy density but suffer from rapid capacity fading due to the layered-to-rock-salt transition of NMC811 and structural degradation of Li6PS5Cl from parasitic interfacial reactions. Here, we demonstrate a catholyte engineering strategy using a Li2S scavenging additive to suppress interfacial reactivity and preserve the structural and electrochemical stability of both NMC811 and Li6PS5Cl. Incorporating 0.10 wt.% Li2S enables exceptional cycling stability, achieving 76% capacity retention after 550 cycles at C/10 and 88% retention after 800 cycles at C/3 at 60 degrees C, compared with rapid failure in pristine cells. Spectroscopic, electrochemical, and morphological analyses confirm that Li2S maintains electrode integrity by sustaining particle contact and suppressing phase decomposition. This work elucidates interfacial degradation pathways in NMC811/argyrodite systems and introduces a low-cost, scalable strategy to stabilize nickel-rich oxide cathodes in ASSLMBs, advancing their practical viability.
Original languageAmerican English
Number of pages12
JournalEnergy Strategy Reviews
Volume86
DOIs
StatePublished - 2026

NLR Publication Number

  • NLR/JA-5700-100925

Keywords

  • all-solid-state batteries
  • argyrodite solid-state electrolytes
  • energy storage
  • nickel-rich lithium-ion cathode materials
  • solid-state electrolytes

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