Digestion processes and elemental analysis of oxide and sulfide solid electrolytes

Thomas F. Malkowski, Ethan D. Boeding, Dina Fattakhova-Rohlfing, Nadine Wettengl, Martin Finsterbusch, Gabriel M. Veith

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

Abstract

Detailed elemental analysis is essential for a successful development and optimization of material systems and synthesis methods. This is especially relevant for Li- and Na-containing compounds, found in state-of-the-art and next-generation battery systems. Their materials’ properties and thus the final device performance strongly depend on the crystal structure, the stoichiometry, and defect chemistry, e.g., influencing charge carrier concentration and activation energies for vacancy transport. However, a detailed quantitative analysis of light elements in a heavy matrix, featuring a broad range of solubilities and vapor pressures, is often difficult and associated with large uncertainties and thus neglected in favor of just reporting the stoichiometry as “weighed in.” In this work, we report several approaches to digest and dissolve various oxide and sulfide-based materials, used in next-generation Li batteries, for elemental analysis via optical emission spectroscopy. These include the most common solid electrolytes Li-La-Ti–O, a perovskite material (LLTO), and Li-La-Zr-O which has garnet structure (LLZO). Additionally, a facile thermal digestion process is reported for a surrogate sulfide solid electrolyte (Na2S). The digestion procedures reported here are suitable for almost any laboratory environment and, when applied, will improve understanding of the synthesis-structure–property correlations needed to advanced batteries with all solid-state configurations.

Original languageEnglish
Pages (from-to)3223-3231
Number of pages9
JournalIonics
Volume28
Issue number7
DOIs
StatePublished - Jul 2022

Funding

The authors would like to thank Dr. Tim Armstrong (Steward Advanced Materials—Chattanooga TN) for the commercial samples of solid electrolytes. GMV would like to thank Diana Stamberga in ORNL’s Chemical Separations Group for repeated access to the ICP used in this work and the high level of safety instilled in her laboratories. Work at ORNL (TFM, EOB, GMV – LLTO, LLZO digestion, NaS) was supported by the U.S. Department of Energy, Office of Science, Basic Energy Sciences, Materials Science and Engineering. Work at Julich was conducted as part of the US-German joint collaboration on “Interfaces and Interphases In Rechargeable Li-metal based Batteries” supported by the US Department of Energy (DOE) and German Federal Ministry of Education and Research (BMBF). Financial support from the BMBF within 03XP0223A. Additionally, funding from the German Federal Ministry of Education and Research (BMBF) under grant no.: 13XP0173A (FestBatt-Oxide) and 13XP0434A (FB2-Oxide) is gratefully acknowledged. This manuscript has been authored by UT-Battelle, LLC, under contract DE-AC05-00OR22725 with the US Department of Energy (DOE). 2 This manuscript has been authored by UT-Battelle, LLC, under contract DE-AC05-00OR22725 with the US Department of Energy (DOE). the U.S. government retains and the publisher, by accepting the article for publication, acknowledges, that the US government retains a nonexclusive, paid-up, irrevocable, worldwide license to publish or reproduce the published form of this manuscript, or allow others to do so, for US government purposes. DOE will provide public access to these results of federally sponsored research in accordance with the DOE Public Access Plan ( https://energy.gov/downloads/doe-public-access-plan )

FundersFunder number
Materials Science and Engineering
U.S. Department of Energy
Office of Science
Basic Energy Sciences
Oak Ridge National Laboratory
Bundesministerium für Bildung und ForschungDE-AC05-00OR22725, 13XP0173A, 03XP0223A, 13XP0434A, FB2-Oxide

    Keywords

    • Chemical analysis
    • Garnet
    • Lithium content

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