2 research outputs found

    Thickness-Dependent Binding Energy Shift in Few-Layer MoS<sub>2</sub> Grown by Chemical Vapor Deposition

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    The thickness-dependent surface states of MoS<sub>2</sub> thin films grown by the chemical vapor deposition process on the SiO<sub>2</sub>–Si substrates are investigated by X-ray photoelectron spectroscopy. Raman and high-resolution transmission electron microscopy suggest the thicknesses of MoS<sub>2</sub> films to be ranging from 3 to 10 layers. Both the core levels and valence band edges of MoS<sub>2</sub> shift downward ∼0.2 eV as the film thickness increases, which can be ascribed to the Fermi level variations resulting from the surface states and bulk defects. Grainy features observed from the atomic force microscopy topographies, and sulfur-vacancy-induced defect states illustrated at the valence band spectra imply the generation of surface states that causes the downward band bending at the n-type MoS<sub>2</sub> surface. Bulk defects in thick MoS<sub>2</sub> may also influence the Fermi level oppositely compared to the surface states. When Au contacts with our MoS<sub>2</sub> thin films, the Fermi level downshifts and the binding energy reduces due to the hole-doping characteristics of Au and easy charge transfer from the surface defect sites of MoS<sub>2</sub>. The shift of the onset potentials in hydrogen evolution reaction and the evolution of charge-transfer resistances extracted from the impedance measurement also indicate the Fermi level varies with MoS<sub>2</sub> film thickness. The tunable Fermi level and the high chemical stability make our MoS<sub>2</sub> a potential catalyst. The observed thickness-dependent properties can also be applied to other transition-metal dichalcogenides (TMDs), and facilitates the development in the low-dimensional electronic devices and catalysts

    Ultraefficient Ultraviolet and Visible Light Sensing and Ohmic Contacts in High-Mobility InSe Nanoflake Photodetectors Fabricated by the Focused Ion Beam Technique

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    A photodetector using a two-dimensional (2D) low-direct band gap indium selenide (InSe) nanostructure fabricated by the focused ion beam (FIB) technique has been investigated. The FIB-fabricated InSe photodetectors with a low contact resistance exhibit record high responsivity and detectivity to the ultraviolet and visible lights. The optimal responsivity and detectivity up to 1.8 × 10<sup>7</sup> A W<sup>–1</sup> and 1.1 × 10<sup>15</sup> Jones, respectively, are much higher than those of the other 2D material-based photoconductors and phototransistors. Moreover, the inherent photoconductivity (PC) quantified by the value of normalized gain has also been discussed and compared. By excluding the contribution of artificial parameters, the InSe nanoflakes exhibit an ultrahigh normalized gain of 3.2 cm<sup>2</sup> V<sup>–1</sup>, which is several orders of magnitude higher than those of MoS<sub>2</sub>, GaS, and other layer material nanostructures. A high electron mobility at room temperature reaching 450 cm<sup>2</sup> V<sup>–1</sup> s<sup>–1</sup> has been confirmed to be one of the major causes of the inherent superior PC in the InSe nanoflakes. The oxygen-sensitized PC mechanism that enhances carrier lifetime and carrier collection efficiency has also been proposed. This work demonstrates the devices fabricated by the FIB technique using InSe nanostructures for highly efficient broad-band optical sensing and light harvesting, which is critical for development of the 2D material-based ultrathin flexible optoelectronics
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