Atomic-Scale Visualization of Electrochemical Lithiation Processes in Monolayer MoS2 by Cryogenic Electron Microscopy

Seung Ho Yu, Michael J. Zachman, Kibum Kang, Hui Gao, Xin Huang, Francis J. DiSalvo, Jiwoong Park, Lena F. Kourkoutis, Héctor D. Abruña

Research output: Contribution to journalArticlepeer-review

34 Scopus citations

Abstract

While lithium ion batteries with electrodes based on intercalation compounds have dominated the portable energy storage market for decades, the energy density of these materials is fundamentally limited. Today, rapidly growing demand for this type of energy storage is driving research into materials that utilize alternative reaction mechanisms to enable higher energy densities. Transition metal compounds are one such class of materials, with storage enabled by “conversion” reactions, where the material is converted to new compound upon lithiation. MoS2 is one example of this type of material that has generated a large amount of interest recently due to its high theoretical lithium storage capacity compared to graphite. Here, cryogenic scanning transmission electron microscopy techniques are used to reveal the atomic-scale processes that occur during reaction of a model monolayer MoS2 system by enabling the unaltered atomic structure to be determined at various levels of lithiation. It is revealed that monolayer MoS2 can undergo a conversion reaction even with no substrate, and that the resulting particles are smaller than those that form in bulk MoS2, likely due to the more limited 2D diffusion. Additionally, while bilayer MoS2 undergoes intercalation with a corresponding phase transition before conversion, monolayer MoS2 does not.

Original languageEnglish
Article number1902773
JournalAdvanced Energy Materials
Volume9
Issue number47
DOIs
StatePublished - Dec 1 2019
Externally publishedYes

Funding

S.-H.Y. and M.J.Z. contributed equally to this work. S.-H.Y. acknowledges support from CHESS and the Energy Materials Center at Cornell (EMC2). M.J.Z. and L.F.K. were primarily supported by the National Science Foundation (NSF) (DMR-1654596) and the Packard Foundation. This work made use of the Cornell Center for Materials Research (CCMR) Shared Facilities with funding from the NSF Materials Research Science and Engineering Centers (MRSEC) program (DMR-1719875). The FEI Titan Themis 300 was acquired through NSF MRI-1429155, with additional support from Cornell University, the Weill Institute, and the Kavli Institute at Cornell. K.K., H.G., and J.P. acknowledge additional support from Air Force Office of Scientific Research (AFOSR) Multidisciplinary Research Program of the University Research Initiative (MURI) (FA9550-16-1-003) and the Platform for the Accelerated Realization, Analysis, and Discovery of Interface Materials (PARADIM) Materials Innovation Platform in-house program by NSF grant DMR-1539918. K.K. acknowledges additional support from the Korea Institute of Science and Technology (KIST) Institutional Program (2V07080-19-P148).

FundersFunder number
Energy Materials Center at Cornell
Kavli Institute at Cornell
Weill Institute
National Science Foundation1719875, 1654596, DMR-1654596
David and Lucile Packard Foundation
Air Force Office of Scientific ResearchDMR-1539918, FA9550-16-1-003
Cornell University
Materials Research Science and Engineering Center, Harvard UniversityDMR-1719875, MRI-1429155
Korea Institute of Science and Technology2V07080-19-P148

    Keywords

    • conversion reaction
    • cryogenic electron microscopy
    • intercalation reaction
    • lithium ion batteries
    • molybdenum disulfide

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