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We report a two-step growth process of MoS nanoflakes using a low-pressure chemical vapor deposition technique. In the first step, a MoS layer was synthesized on a c-plane sapphire substrate. This layer was subsequently re-evaporated at a higher temperature to form mono- or few-layer MoS flakes. As a result, the close proximity re-evaporation enabled the growth of pristine MoS nanoflakes. Atomic force microscopy analysis confirmed the synthesis of nanoclusters/nanoflakes with lateral dimensions of over 10 μm and a flake height of approximately 1.3 nm, demonstrating bi-layer MoS, whereas transmission electron microscopy analysis revealed triangular MoS nanoflakes, with a diffraction pattern proving the presence of single crystalline hexagonal MoS. Raman data revealed the typical modes of high-quality MoS nanoflakes. Finally, we presented the photocurrent dependence of a MoS-based photoresist under illumination with light-emitting diode of 405 nm wavelength. The measured current-voltage dependence across various luminous flux outlined the sensitivity of MoS to polarized light and thus opens further opportunities for applications in high-performance photodetectors with polarization sensitivity.
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http://dx.doi.org/10.3390/nano14141213 | DOI Listing |
ACS Catal
August 2025
Department of Chemistry "U. Schiff" (DICUS), University of Florence and INSTM unit, Via della Lastruccia 3-13, Sesto Fiorentino, Florence 50019, Italy.
The surface functionalization of chemically exfoliated MoS (-MoS) nanoflakes with Brønsted-acid end-capped aryl fragments adds an additional level of complexity to the comprehension of the correlation between the electron-donating strength of covalently grafted organic groups (Hammett parameter) and the HER performance of these hybrids. MoS nanoflakes decorated with aryl-sulfonic acids promote proton transfer via tunneling of H-species, where weaker benzoic acid groups fail. Thus, surface-engineered -MoS bearing sulfonic-acid end-capped dangling arms acts as an electrocatalyst that boosts HER kinetics even under an alkaline environment, where water dissociation represents the bottleneck of the process.
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July 2025
Department of Chemistry, Herbal Medicines Raw Materials Research Center, Shahrood Branch, Islamic Azad University, Shahrood, Iran.
MoS₂ nanoflakes are emerging as a promising material for photothermal therapy due to their high absorption in the NIR region, large specific surface area, biocompatibility, efficient photothermal conversion, and ability to be functionalized for targeted therapy. In this paper, MoS₂ nanoflakes were incorporated to FeO nanoparticles, gold nanorod (GNR), and copper sulfide (CuS) (MCG nanocomposite) to investigate chemo-photothermal therapy in this nanocomposite. The structural and optical properties of the MCG nanocomposite were characterized by X-ray diffraction (XRD), Transmission electron microscopy (TEM), Zeta potential, Dynamic Light Scattering (DLS), Fourier transform infrared (FTIR), and Ultraviolet-visible (UV-Vis) spectroscopies.
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July 2025
Catalan Institute of Nanoscience and Nanotechnology (ICN2), CSIC and BIST, Campus UAB, Bellaterra, E-08193, Barcelona, Spain.
Nanostructures based on transition metal dichalcogenides have attracted considerable attention due to their tunable optoelectronic properties and large surface areas, showing a great potential as photocatalysts. Here, a novel supported structure based on 2D-MoS/CuO nanoflakes grown on 3D mesoporous silica templates fabricated by a combination of solvothermal synthesis and e-beam deposition methods is presented. The synthesized MoS nanoflakes exhibited a combination of trigonal-prismatic 2H and distorted-trigonal 1T' phases, which contributed to a high density of active catalytic sites, facilitating efficient photogenerated charge transfer to analytes at the liquid interface.
View Article and Find Full Text PDFACS Appl Mater Interfaces
April 2025
School of Resource and Environmental Science, Wuhan University, Wuhan 430072, P. R. China.
A facile synthesis process that facilitates the industrial-scale production of catalysts is the prerequisite of the hydrogen evolution reaction (HER) industry. Molybdenum-based catalysts are ideal alternatives for precious-metal-based HER materials; however, they remain challenging in scale-up preparation due to the costly and complex Mo sources. Herein, we propose a molten salt paired electrolysis approach to synthesize transition-metal-doped MoC catalysts directly from molybdenite (mainly consisting of micrometer-scale MoS bulks), an earth-abundant natural Mo ore.
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