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Control of Two Solid Electrolyte Interphases at the Negative Electrode of an Anode-Free All Solid-State Battery based on Argyrodite Electrolyte

  • Yixian Wang
  • , Vikalp Raj
  • , Kaustubh G. Naik
  • , Bairav S. Vishnugopi
  • , Jaeyoung Cho
  • , Mai Nguyen
  • , Elizabeth A. Recker
  • , Yufeng Su
  • , Hugo Celio
  • , Andrei Dolocan
  • , Zachariah A. Page
  • , John Watt
  • , Graeme Henkelman
  • , Qingsong Howard Tu
  • , Partha P. Mukherjee
  • , David Mitlin

Research output: Contribution to journalArticlepeer-review

14 Scopus citations

Abstract

Anode-free all solid-state batteries (AF-ASSBs) employ “empty” current collector with three active interfaces that determine electrochemical stability; lithium metal – Solid electrolyte (SE) interphase (SEI-1), lithium – current collector interface, and collector – SE interphase (SEI-2). Argyrodite Li6PS5Cl (LPSCl) solid electrolyte (SE) displays SEI-2 containing copper sulfides, formed even at open circuit. Bilayer of 140 nm magnesium/30 nm tungsten (Mg/W-Cu) controls the three interfaces and allows for state-of-the-art electrochemical performance in half-cells and fullcells. AF-ASSB with NMC811 cathode achieves 150 cycles with Coulombic efficiency (CE) above 99.8%. With high mass-loading cathode (8.6 mAh cm−2), AF-ASSB retains 86.5% capacity after 45 cycles at 0.2C. During electrodeposition of Li, gradient Li-Mg solid solution is formed, which reverses upon electrodissolution. This promotes conformal wetting/dewetting by Li and stabilizes SEI-1 by lowering thermodynamic driving force for SE reduction. Inert refractory W underlayer is required to prevent ongoing formation of SEI-2 that also drives electrochemical degradation. Inert Mo and Nb layers likewise protect Cu from corroding, while Li-alloying layers (Mg, Sn) are less effective due to ongoing volume changes and associated pulverization. Mechanistic explanation for observed Li segregation within alloying LixMg layer is provided through mesoscale modelling, considering opposing roles of diffusivity differences and interfacial stresses.

Original languageEnglish
Article number2410948
JournalAdvanced Materials
Volume37
Issue number11
DOIs
StatePublished - Mar 19 2025
Externally publishedYes

Funding

Y.W. and D.M. were supported by the Assistant Secretary for Energy Efficiency and Renewable Energy, Office of Vehicle Technologies of the U.S. Department of Energy (DOE) through the Advanced Battery Materials Research Program (Battery500 Consortium). V.R., K.G.N., B.S.V., and P.P.M. were supported by the Mechano-Chemical Understanding of Solid Ion Conductors, an Energy Frontier Research Center funded by the U.S. Department of Energy, Office of Science, Office of Basic Energy Science, contact DE-SC0023438. E.A.R. and Z.A.P. were supported by The Welch Foundation under Grant No. F-2007 (nanoindentation characterization) and E.A.R. was supported by the National Science Foundation (NSF) Division of Graduate Education (DGE) through the Graduate Research Fellowship Program under Grant No. 2137420. The acquisition of XPS was supported by the National Science Foundation Major Research Instrumentation program (Grant No. 2117623). This work was performed, in part, at the Center for Integrated Nanotechnologies, an Office of Science User Facility operated by the U.S. Department of Energy (DOE) Office of Science. Los Alamos National Laboratory, an affirmative action equal opportunity employer, is managed by Triad National Security, LLC for the U.S. Department of Energy's NNSA, under contract 89233218CNA000001. J.C., M.N., and G.H. were supported by Texas Advanced Computing Center (TACC) and Advanced Cyberinfrastructure Coordination Ecosystem: Services and Support (ACCESS) – CHE190010. This work was supported by The Welch Foundation (F-2206). Y.W. and D.M. were supported by the Assistant Secretary for Energy Efficiency and Renewable Energy, Office of Vehicle Technologies of the U.S. Department of Energy (DOE) through the Advanced Battery Materials Research Program (Battery500 Consortium). V.R., K.G.N., B.S.V., and P.P.M. were supported by the Mechano‐Chemical Understanding of Solid Ion Conductors, an Energy Frontier Research Center funded by the U.S. Department of Energy, Office of Science, Office of Basic Energy Science, contact DE‐SC0023438. E.A.R. and Z.A.P. were supported by The Welch Foundation under Grant No. F‐2007 (nanoindentation characterization) and E.A.R. was supported by the National Science Foundation (NSF) Division of Graduate Education (DGE) through the Graduate Research Fellowship Program under Grant No. 2137420. The acquisition of XPS was supported by the National Science Foundation Major Research Instrumentation program (Grant No. 2117623). This work was performed, in part, at the Center for Integrated Nanotechnologies, an Office of Science User Facility operated by the U.S. Department of Energy (DOE) Office of Science. Los Alamos National Laboratory, an affirmative action equal opportunity employer, is managed by Triad National Security, LLC for the U.S. Department of Energy's NNSA, under contract 89233218CNA000001. J.C., M.N., and G.H. were supported by Texas Advanced Computing Center (TACC) and Advanced Cyberinfrastructure Coordination Ecosystem: Services and Support (ACCESS) – CHE190010. This work was supported by The Welch Foundation (F‐2206).

Keywords

  • all-solid-state battery (ASSB)
  • anode-free battery
  • cryogenic microscopy
  • solid-state electrolyte (SE)
  • sulfide electrolyte

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