Aqueous Zinc-Ion Storage in MoS2 by Tuning the Intercalation Energy
Anjum, Dalaver H.
Alshareef, Husam N.
KAUST DepartmentChemical Science Program
Functional Nanomaterials and Devices Research Group
Imaging and Characterization Core Lab
KAUST Catalysis Center (KCC)
Material Science and Engineering Program
Physical Science and Engineering (PSE) Division
KAUST Grant NumberOSR-CRG2018-3735
Online Publication Date2019-04-15
Print Publication Date2019-05-08
Permanent link to this recordhttp://hdl.handle.net/10754/631963
MetadataShow full item record
AbstractAqueous Zn-ion batteries present low-cost, safe, and high-energy battery technology but suffer from the lack of suitable cathode materials because of the sluggish intercalation kinetics associated with the large size of hydrated zinc ions. Herein we report an effective and general strategy to transform inactive intercalation hosts into efficient Zn2+ storage materials through intercalation energy tuning. Using MoS2 as a model system, we show both experimentally and theoretically that even hosts with an originally poor Zn2+ diffusivity can allow fast Zn2+ diffusion. Through simple interlayer spacing and hydrophilicity engineering that can be experimentally achieved by oxygen incorporation, the Zn2+ diffusivity is boosted by 3 orders of magnitude, effectively enabling the otherwise barely active MoS2 to achieve a high capacity of 232 mAh g–1, which is 10 times that of its pristine form. The strategy developed in our work can be generally applied for enhancing the ion storage capacity of metal chalcogenides and other layered materials, making them promising cathodes for challenging multivalent ion batteries.
CitationLiang H, Cao Z, Ming F, Zhang W, Anjum DH, et al. (2019) Aqueous Zinc-Ion Storage in MoS2 by Tuning the Intercalation Energy. Nano Letters. Available: http://dx.doi.org/10.1021/acs.nanolett.9b00697.
SponsorsThe work reported in this manuscript was supported by King Abdullah University of Science and Technology (KAUST) under grant number OSR-CRG2018-3735. The calculations were performed on the KAUST HPC supercomputers.
PublisherAmerican Chemical Society (ACS)