Journal
SMALL METHODS
Volume -, Issue -, Pages -Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/smtd.202300503
Keywords
composite electrodes; lithium-ion batteries; MAX phase; negative electrodes; tin; titanium oxide
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This study develops composite electrodes based on the (Ti/Sn)O-2 system through partial oxidation of the tin-containing MAX phase. These electrodes exhibit excellent mechanical stability and high specific capacities. The intimate contact between the MAX phase and oxide particles, as revealed by chemical, morphological, and structural investigation, explains the unprecedented electrochemical performances. The unreacted MAX phase acts as a conductive agent and a buffer to maintain the mechanical integrity of the oxide during lithiation and delithiation cycles.
Among the materials for the negative electrodes in Li-ion batteries, oxides capable of reacting with Li+ via intercalation/conversion/alloying are extremely interesting due to their high specific capacities but suffer from poor mechanical stability. A new way to design nanocomposites based on the (Ti/Sn)O-2 system is the partial oxidation of the tin-containing MAX phase of Ti3Al(1-x)SnxO2 composition. Exploiting this strategy, this work develops composite electrodes of (Ti/Sn)O-2 and MAX phase capable of withstanding over 600 cycles in half cells with charge efficiencies higher than 99.5% and specific capacities comparable to those of graphite and higher than lithium titanate (Li4Ti5O12) or MXenes electrodes. These unprecedented electrochemical performances are also demonstrated at full cell level in the presence of a low cobalt content layered oxide and explained through an accurate chemical, morphological, and structural investigation which reveals the intimate contact between the MAX phase and the oxide particles. During the oxidation process, electroactive nanoparticles of TiO2 and Ti(1-y)SnyO2 nucleate on the surface of the unreacted MAX phase which therefore acts both as a conductive agent and as a buffer to preserve the mechanical integrity of the oxide during the lithiation and delithiation cycles.
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