4.6 Article

Layer-stacking of chalcogenide-terminated MXenes Ti2CT2(T = O, S, Se, Te) and their applications in metal-ion batteries

Journal

NANOTECHNOLOGY
Volume 34, Issue 10, Pages -

Publisher

IOP Publishing Ltd
DOI: 10.1088/1361-6528/aca9d7

Keywords

MXenes; metal-ion batteries; first-principles calculations; electrodes; electronic structures

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Due to limited supply of lithium, the development of non-Li-ion batteries has become a research focus. In this study, the performance of chalcogenide-terminated MXenes as electrodes for Li-ion and non-Li-ion batteries was investigated using first-principles calculations. Different stacking types were observed in O/Te and S/Se terminated Ti2C multilayers. Ti2CO2 was found to be a potential anode material for Na- and K-ion batteries, while Ti2CS2 and Ti2CSe2 showed promise for Na-, K-, and Ca-ion batteries. Among these materials, Ti2CS2 exhibited the highest ion capacity of 616 mAh g(-1). These findings may inspire further experimental and theoretical studies of Ti2C-MXenes as electrodes for metal-ion batteries.
Owning to limited supply of lithium for Li-ion batteries, the development of non-Li-ion batteries (such as Na+, K+ Mg2+, Ca2+, and Al3+ ion batteries) has attracted significant research interest. In this work, by means of the first-principles calculations, we systematically investigated the performance of chalcogenide-terminated MXenes Ti2CT2 (T = O, S, Se, and Te) as electrodes for Li-ion and non-Li-ion batteries, as well as the layer-stacking and electronic properties of Ti2CT2. We find that the stacking type of O and Te terminated Ti2C multilayers with AA stacking differs from that of S and Se terminated Ti2C multilayers with AB stacking. More importantly, Ti2CO2 monolayer can be potential anode material for Na- and K-ion batteries with high capacities and very low diffusion barriers (0.03-0.11 eV), while Ti2CS2 and Ti2CSe2 are promising anode materials with relatively low average open circuit voltages (OCVs) for Na-, K-, and Ca-ion batteries (0.4-0.87 V). Among these materials, Ti2CS2 exhibits the largest ion capacity of 616 mAh g(-1). These results of our work may inspire further studies of Ti2C-MXenes multilayers as electrodes for metal-ion batteries either experimentally or theoretically.

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