A highly efficient, reproducible, and scalable approach for exfoliation of MoS2 is critical for utilizing these emerging materials from coatings and composites to printable devices. Additive-free techniques, such as solvent-assisted exfoliation via sonication, are considered to be the most viable approach, where N-methyl-2-pyrrolidone (NMP) is the most effective solvent. However, understanding the mechanism of exfoliation and the key role NMP plays during the process have been elusive and challenges effective improvements in product yield and quality. Here, we report systematic experiments to understand the mechanism of solvent-assisted exfoliation by elucidating the sonolysis chemistries associated with NMP. It is confirmed that in the presence of O2(g) dissolved moisture in NMP plays a critical role during sonication. The higher the moisture content, the more efficient the exfoliation process is. Conversely, when exfoliations are carried out with dried solvents with an inert atmosphere, reaction yields decrease. This is due to redox-active species formed in situ through an autoxidation pathway that converts NMP to N-methyl succinimide by hydroperoxide intermediates. These highly reactive species appear to aid exfoliation by oxidation at reactive edge sites; the charging creates Coulombic repulsion between neighboring sheets that disrupts interlayer basal plane bonding and enables electrostatic stabilization of particles in high-dipole solvents. From these insights, exfoliation in previously reported inactive solvents (e.g., acetonitrile), as well as in the absence of probe sonication, is demonstrated. These findings illustrate that exfoliation of MoS2, and possibly TMD’s in general, can be mediated through understanding the chemistry occurring at the surface–solvent interface.

The synergy of self- and directed-assembly processes and lithography provides intriguing avenues to fabricate translationally ordered nanoparticle arrangements, but currently lacks the robustness necessary to deliver complex spatial organization. Here, we demonstrate that interparticle spacing and local orientation of gold nanorods (AuNR) can be tuned by controlling the Debye length of AuNR in solution and the dimensions of a chemical contrast pattern. Electrostatic and hydrophobic selectivity for AuNR to absorb to patterned regions of poly(2-vinylpyridine) (P2VP) and polystyrene brushes and mats was demonstrated for AuNR functionalized with mercaptopropane sulfonate (MS) and poly(ethylene glycol), respectively. For P2VP patterns of stripes with widths comparable to the length of the AuNR, single- and double-column arrangements of AuNR oriented parallel and perpendicular to the P2VP line were obtained for MS-AuNR. Furthermore, the spacing of the assembled AuNR was uniform along the stripe and related to the ionic strength of the AuNR dispersion. The different AuNR arrangements are consistent with predictions based on maximization of packing of AuNR within the confined strip.

Uniform growth of pristine two dimensional (2D) materials over large areas at lower temperatures without sacrifice of their unique physical properties is a critical pre-requisite for seamless integration of next-generation van der Waals heterostructures into functional devices. This Letter describes a vapor phase growth technique for precisely controlled synthesis of continuous, uniform molecular layers of MoS2 on silicon dioxide and highly oriented pyrolitic graphite substrates of over several square centimeters at 350 °C. Synthesis of few-layer MoS2 in this ultra-high vacuum physical vapor deposition process yields materials with key optical and electronic properties identical to exfoliated layers. The films are composed of nano-scale domains with strong chemical binding between domain boundaries, allowing lift-off from the substrate and electronic transport measurements from contacts with separation on the order of centimeters.

Nanoscale ionic materials (NIMS) are organic-inorganic hybrids in which a core nanostructure is functionalized with a covalently attached corona and an ionically tethered organic canopy. NIMS are engineered to be liquids under ambient conditions in the absence of solvent and are of interest for a variety of applications. We have used nuclear magnetic resonance (NMR) relaxation and pulse-field gradient (PFG) diffusion experiments to measure the canopy dynamics of NIMS prepared from 18-nm silica cores modified by an alkylsilane monolayer possessing terminal sulfonic