Removal and Reoccurrence of LLZTO Surface Contaminants under Glovebox Conditions
Source abstract
Abstract
High Resolution Image Download MS PowerPoint Slide The reactivity of Li 6.4 La 3 Zr 1.4 Ta 0.6 O 12 (LLZTO) solid electrolytes to form lithio-phobic species such as Li 2 CO 3 on their surface when exposed to trace amounts of H 2 O and CO 2 limits the progress of LLZTO-based solid-state batteries. Various treatments, such as annealing LLZTO within a glovebox or acid etching, aim at removing the surface contaminants, but a comprehensive understanding of the evolving LLZTO surface chemistry during and after these treatments is lacking. Here, glovebox-like H 2 O and CO 2 conditions were recreated in a near ambient pressure X-ray photoelectron spectroscopy chamber to analyze the LLZTO surface under realistic conditions. We find that annealing LLZTO at 600 °C in this atmosphere effectively removes the surface contaminants, but a significant level of contamination reappears upon cooling down. In contrast, HCl (aq) acid etching demonstrates superior Li 2 CO 3 removal and stable surface chemistry post treatment. To avoid air exposure during the acid treatment, an anhydrous HCl solution in diethyl ether was used directly within the glovebox. This novel acid etching strategy delivers the lowest lithium/LLZTO interfacial resistance and the highest critical current density.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Battery Technologies Research · Advancements in Battery Materials · Advanced Battery Materials and Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials, University of Oxford, Oxford OX1 3PH, U.K.
The Faraday Institution, Didcot OX11 0RA, U.K.
School of Chemistry, University of Edinburgh, Edinburgh EH9 3FJ, U.K.
Diamond Light Source, Didcot OX11 0DE, U.K.
Funding
Engineering and Physical Sciences Research Council · UK Research and Innovation · Faraday Institution · H2020 European Research Council
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