Understanding the Surface Regeneration and Reactivity of Garnet Solid-State Electrolytes
Source abstract
Abstract
High Resolution Image Download MS PowerPoint Slide Garnet solid-electrolyte-based Li-metal batteries can be used in energy storage devices with high energy densities and thermal stability. However, the tendency of garnets to form lithium hydroxide and carbonate on the surface in an ambient atmosphere poses significant processing challenges. In this work, the decomposition of surface layers under various gas environments is studied by using two surface-sensitive techniques, near-ambient-pressure X-ray photoelectron spectroscopy and grazing incidence X-ray diffraction. It is found that heating to 500 °C under an oxygen atmosphere (of 1 mbar and above) leads to a clean garnet surface, whereas low oxygen partial pressures (i.e., in argon or vacuum) lead to additional graphitic carbon deposits. The clean surface of garnets reacts directly with moisture and carbon dioxide below 400 and 500 °C, respectively. This suggests that additional CO 2 concentration controls are needed for the handling of garnets. By heating under O 2 along with avoiding H 2 O and CO 2, symmetric cells with less than 10 Ωcm 2 interface resistance are prepared without the use of any interlayers; plating currents of >1 mA cm –2 without dendrite initiation are demonstrated.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Battery Materials and Technologies · Advancements in Battery Materials · Thermal Expansion and Ionic Conductivity
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Yusuf Hamied Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, United Kingdom
The Faraday Institution, Quad One, Harwell Campus, Didcot OX11 0RA, United Kingdom
Diamond Light Source, Harwell Science and Innovation Campus, Didcot OX11 ODE, United Kingdom
Fakultät Physik/DELTA, Technische Universität Dortmund, 44221 Dortmund, Germany
Funding
Royal Society · Science and Engineering Research Board · Faraday Institution · H2020 European Research Council
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