Molybdenum disulfide (MoS) transistors are a promising alternative for the semiconductor industry due to their large on/off current ratio (>10), immunity to short-channel effects, and unique switching characteristics. MoS has drawn considerable interest due to its intriguing electrical, optical, sensing, and catalytic properties. Monolayer MoS is a semiconducting material with a direct band gap of ~1.9 eV, which can be tuned. Commercially, the aim of synthesizing a novel material is to grow high-quality samples over a large area and at a low cost. Although chemical vapor deposition (CVD) growth techniques are associated with a low-cost pathway and large-area material growth, a drawback concerns meeting the high crystalline quality required for nanoelectronic and optoelectronic applications. This research presents a lower-temperature CVD for the repeatable synthesis of large-size mono- or few-layer MoS using the direct vapor phase sulfurization of MoO. The samples grown on Si/SiO substrates demonstrate a uniform single-crystalline quality in Raman spectroscopy, photoluminescence (PL), scanning electron microscopy (SEM), atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS), and scanning transmission electron microscopy. These characterization techniques were targeted to confirm the uniform thickness, stoichiometry, and lattice spacing of the MoS layers. The MoS crystals were deposited over the entire surface of the sample substrate. With a detailed discussion of the CVD setup and an explanation of the process parameters that influence nucleation and growth, this work opens a new platform for the repeatable synthesis of highly crystalline mono- or few-layer MoS suitable for optoelectronic application.
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http://dx.doi.org/10.3390/mi14091758 | DOI Listing |
Chemphyschem
November 2024
Department of Chemistry, University of Central Florida, Orlando, Florida, 32816, USA.
2D materials have rapidly become the building blocks for the next generation of semiconducting materials and devices, with chemical vapor deposition (CVD) emerging as a prefered method for their synthesis. However, the predictable and reproducible growth of high quality, large 2D monolayers remains challenging. An important facet is controlling the local environment at the surface of the substrate - here, space-confinement techniques have emerged as promising candidates.
View Article and Find Full Text PDFIn this Letter, we report TAMM plasmonic polaritons (TPPs) generated by few-layer MoS with a distributed Bragg reflector (DBR) structure in the terahertz frequency region by utilizing the transfer matrix method (TMM) and finite element method (FEM). By inserting a mono-graphene embedded cavity layer, we realize the graphene-induced mode strong coupling (GCM), which is a strategy of a refractive index sensor by optimizing the cavity layer spacing. By adjusting the chemical potential of graphene, GCM is modulated.
View Article and Find Full Text PDFNature
September 2024
Cavendish Laboratory, University of Cambridge, Cambridge, UK.
Crystallographic phase engineering plays an important part in the precise control of the physical and electronic properties of materials. In two-dimensional transition metal dichalcogenides (2D TMDs), phase engineering using chemical lithiation with the organometallization agent n-butyllithium (n-BuLi), to convert the semiconducting 2H (trigonal) to the metallic 1T (octahedral) phase, has been widely explored for applications in areas such as transistors, catalysis and batteries. Although this chemical phase engineering can be performed at ambient temperatures and pressures, the underlying mechanisms are poorly understood, and the use of n-BuLi raises notable safety concerns.
View Article and Find Full Text PDFNanomaterials (Basel)
July 2024
Institute of Optical Materials and Technologies, Bulgarian Academy of Sciences, 1113 Sofia, Bulgaria.
Adv Mater
September 2024
Innovative Functional Materials Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Nagoya, 463-8560, Japan.
Superatomic clusters - assemblies of atoms with various sizes, shapes, and compositions - can form hierarchical architectures that exhibit emergent electronic properties not found in their individual units. In particular, cubic MX clusters of chalcogenides (M = transition metal; X = chalcogen) are recognized as versatile building blocks for 3D structures with tunable morphologies and electronic properties. However, tetrahedral MX clusters rarely assemble into 2D architectures, which could offer a distinct class of functional materials from their 3D analogues.
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