SnO2 Model Electrode Cycled in Li-Ion Battery Reveals the Formation of Li2SnO3 and Li8SnO6 Phases through Conversion Reactions
Source abstract
Abstract
SnO2 is an attractive negative electrode for Li-ion battery owing to its high specific charge compared to commercial graphite. However, the various intermediate conversion and alloy reactions taking place during lithiation/delithiation, as well as the electrolyte stability, have not been fully elucidated, and many ambiguities remain. An amorphous SnO2 thin film was investigated for use as a model electrode by a combination of postmortem X-ray photoelectron spectroscopy supported by density functional theory calculations and scanning electron microscopy to shed light on these different processes. The early stages of lithiation reveal the presence of multiple overlapping reactions leading to the formation of Li2SnO3 and Sn0 phases between 2 and 0.8 V vs Li+/Li. Between 0.45 V and 5 mV vs Li+/Li Li8SnO6, Li2O and Li xSn phases are formed. Electrolyte reduction occurs simultaneously in two steps, at 1.4 and 1 V vs Li+/Li, corresponding to the decomposition of the LiPF6 salt and ethylene carbonate/dimethyl carbonate solvents, respectively. Most of the reactions during delithiation are reversible up to 1.5 V vs Li+/Li, with the reappearance of Sn0 accompanied by the decomposition of Li2O. Above 1.5 V vs Li+/Li, Sn0 is partially reoxidized to SnO x. This process tends to limit the conversion reactions in favor of the alloy reaction, as also confirmed by the long-term cycling samples.
Source: europepmc · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Extraction and Separation Processes
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Faculty of Chemical Engineering and Technology, Krakow University of Technology, 31-155 Krakow, Poland
Funding
Kompetenzzentrum für Energie und Mobilität · Swiss Electric Research
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