Intercalation of alkali atoms within the lamellar transition metal dichalcogenides is a possible route toward a new generation of batteries. It is also a way to induce structural phase transitions authorizing the realization of optical and electrical switches in this class of materials. The process of intercalation has been mostly studied in three-dimensional dichalcogenide films. Here, we address the case of a single-layer of molybdenum disulfide (MoS2), deposited on a gold substrate, and intercalated with cesium (Cs) in ultraclean conditions (ultrahigh vacuum). We show that intercalation decouples MoS2 from its substrate. We reveal electron transfer from Cs to MoS2, relative changes in the energy of the valence band maxima, and electronic disorder induced by structural disorder in the intercalated Cs layer. Besides, we find an abnormal lattice expansion of MoS2, which we relate to immediate vicinity of Cs. Intercalation is thermally activated, and so is the reverse process of deintercalation. Our work opens the route to a microscopic understanding of a process of relevance in several possible future technologies, and shows a way to manipulate the properties of two-dimensional dichalcogenides by "under-cover" functionalization.

Decoupling Molybdenum Disulfide from Its Substrate by Cesium Intercalation

Roberto Sant;
2020-01-01

Abstract

Intercalation of alkali atoms within the lamellar transition metal dichalcogenides is a possible route toward a new generation of batteries. It is also a way to induce structural phase transitions authorizing the realization of optical and electrical switches in this class of materials. The process of intercalation has been mostly studied in three-dimensional dichalcogenide films. Here, we address the case of a single-layer of molybdenum disulfide (MoS2), deposited on a gold substrate, and intercalated with cesium (Cs) in ultraclean conditions (ultrahigh vacuum). We show that intercalation decouples MoS2 from its substrate. We reveal electron transfer from Cs to MoS2, relative changes in the energy of the valence band maxima, and electronic disorder induced by structural disorder in the intercalated Cs layer. Besides, we find an abnormal lattice expansion of MoS2, which we relate to immediate vicinity of Cs. Intercalation is thermally activated, and so is the reverse process of deintercalation. Our work opens the route to a microscopic understanding of a process of relevance in several possible future technologies, and shows a way to manipulate the properties of two-dimensional dichalcogenides by "under-cover" functionalization.
2020
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11311/1253758
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