Thin sheets and small MoS2 nanoparticles have been obtained by exfoliation/fragmentation processes via intense ultrasound cavitation in isopropyl alcohol (IPA). The formation mechanism, the structure (in terms of size, presence of defects, lattice periodicity) and the optical and vibrational properties of the obtained materials have been investigated by means of atomic force (AFM) and high-resolution transmission electron (HRTEM) microscopies and UV–visible near infrared (UV–vis–NIR) and diffuse reflectance infrared Fourier transform (DRIFT) spectroscopies. Fast-Fourier transform (FFT) analyses of HRTEM images have provided a simple and powerful tool to better evidentiate defective situations on extended and regular regions of exfoliated MoS2 nanosheets with large lateral dimensions. The transparent ultracentrifuged portion of MoS2 in IPA is characterized by size and height distributions peaking at about 6 and 1.5 nm, respectively, a fact which is indicative of very high fragmentation and very reduced stacking. The evolution of the UV–vis–NIR and DRIFT spectra upon increasing sonication time and ultracentrifugation give unprecedented information on the optical properties of nanoparticles, on the vibrational properties of surface species, and on the lattice modes of virgin and fragmented material. It is also demonstrated that the extensive layer fragmentation due to the cavitation field is associated with rupture of MoSMo bonds and subsequent exposure of coordinatively and chemically unsaturated Mo and S species. These chemically unsaturated species readily react with the IPA solvent and with atmospheric oxygen with the predominant formation of surface hydroxyl, alkyl, and, to a lesser extent, oxidized species like sulfate and carbonylic and carboxylate groups. Hence, it is concluded that the edges formed by layers breaking in the IPA solution are fully functionalized. This spectroscopic study is made possible by the complete absence of adsorbed IPA, which being a low boiling solvent can be easily removed from MoS2 and does not interfere in the DRIFT measurements. The transparent fraction containing the fragmented particles can be used for blending MoS2 nanoparticles with high surface area materials. This process is favored by the volatile character of IPA, which can be easily removed from the ultrasonicated material. This makes the proposed method fully suitable to prepare MoS2-based hybrid composite materials by simple impregnation of high surface area supports.

Optical, Vibrational, and Structural Properties of MoS2 Nanoparticles Obtained by Exfoliation and Fragmentation via Ultrasound Cavitation in Isopropyl Alcohol.

MUSCUSO, LUCIA;CRAVANZOLA, SARA;CESANO, Federico;SCARANO, Domenica;ZECCHINA, Adriano
2015-01-01

Abstract

Thin sheets and small MoS2 nanoparticles have been obtained by exfoliation/fragmentation processes via intense ultrasound cavitation in isopropyl alcohol (IPA). The formation mechanism, the structure (in terms of size, presence of defects, lattice periodicity) and the optical and vibrational properties of the obtained materials have been investigated by means of atomic force (AFM) and high-resolution transmission electron (HRTEM) microscopies and UV–visible near infrared (UV–vis–NIR) and diffuse reflectance infrared Fourier transform (DRIFT) spectroscopies. Fast-Fourier transform (FFT) analyses of HRTEM images have provided a simple and powerful tool to better evidentiate defective situations on extended and regular regions of exfoliated MoS2 nanosheets with large lateral dimensions. The transparent ultracentrifuged portion of MoS2 in IPA is characterized by size and height distributions peaking at about 6 and 1.5 nm, respectively, a fact which is indicative of very high fragmentation and very reduced stacking. The evolution of the UV–vis–NIR and DRIFT spectra upon increasing sonication time and ultracentrifugation give unprecedented information on the optical properties of nanoparticles, on the vibrational properties of surface species, and on the lattice modes of virgin and fragmented material. It is also demonstrated that the extensive layer fragmentation due to the cavitation field is associated with rupture of MoSMo bonds and subsequent exposure of coordinatively and chemically unsaturated Mo and S species. These chemically unsaturated species readily react with the IPA solvent and with atmospheric oxygen with the predominant formation of surface hydroxyl, alkyl, and, to a lesser extent, oxidized species like sulfate and carbonylic and carboxylate groups. Hence, it is concluded that the edges formed by layers breaking in the IPA solution are fully functionalized. This spectroscopic study is made possible by the complete absence of adsorbed IPA, which being a low boiling solvent can be easily removed from MoS2 and does not interfere in the DRIFT measurements. The transparent fraction containing the fragmented particles can be used for blending MoS2 nanoparticles with high surface area materials. This process is favored by the volatile character of IPA, which can be easily removed from the ultrasonicated material. This makes the proposed method fully suitable to prepare MoS2-based hybrid composite materials by simple impregnation of high surface area supports.
2015
119
7
3791
3801
Few-layer MoS2; MoS2 nanoclusters; Liquid phase exfoliation; UV-vis spectroscopy; IR spectroscopy; atomic force microscopy; transmission electron microscopy; High-resolution transmission electron microscopy; HRTEM; TEM; AFM; MoS2
Lucia Muscuso; Sara Cravanzola; Federico Cesano ;Domenica Scarano ;Adriano Zecchina
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/1508829
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