Synthesis of Rhenium-Doped Molybdenum Sulfide by Atmospheric Pressure Chemical Vapor Deposition (CVD) for a High-Performance Photodetector.

Two-dimensional layered materials have attracted tremendous attention as photodetectors due to their fascinating features, including comprehensive coverage of band gaps, high potential in new-generation electronic devices, mechanical flexibility, and sensitive light-mass interaction. Currently, graphene and transition-metal dichalcogenides (TMDCs) are the most attractive active materials for constructing photodetectors. A growing number of emerging TMDCs applied in photodetectors bring up opportunities in the direct band gap independence with thickness. This study demonstrated for the first time a photodetector based on a few-layer Re x Mo1-x S2, which was grown by chemical vapor deposition (CVD) under atmospheric pressure. The detailed material characterizations were performed using Raman spectroscopy, photoluminescence, and X-ray photoelectron spectroscopy (XPS) on an as-grown few-layer Re x Mo1-x S2. The results show that both MoS2 and ReS2 peaks appear in the Re x Mo1-x S2 Raman diagram. Re x Mo1-x S2 is observed to emit light at a wavelength of 716.8 nm. The electronic band structure of the few layers of Re x Mo1-x S2 calculated using the first-principles theory suggests that the band gap of Re x Mo1-x S2 is larger than that of ReS2 and smaller than that of MoS2, which is consistent with the photoluminescence results. The thermal stability of the few layers of Re x Mo1-x S2 was evaluated using Raman temperature measurements. It is found that the thermal stability of Re x Mo1-x S2 is close to those of pure ReS2 and MoS2. The fabricated Re x Mo1-x S2 photodetector shows a high response rate of 7.46 A W-1 under 365 nm illumination, offering a competitive performance to the devices based on TMDCs and graphenes. This study unambiguously distinguishes Re x Mo1-x S2 as a future candidate in electronics and optoelectronics.

Growth and photocatalytic behavior of transparent reduced GO-ZnO nanocomposite sheets.

Reduced graphene oxide-zinc oxide (rGO-ZnO) nanocomposites were grown on solid substrates by rapid thermal treatment of Langmuir-Blodgett transferred GO-Zn composite sheets in oxygen ambient. The changes induced by uptake of Zn2+ ions and subsequent thermal treatment on surface morphology, micro-structure, composition and optical properties of composite sheets were investigated by atomic force microscopy, high resolution transmission electron microscopy (HR-TEM), X-ray photoelectron spectra (XPS), Fourier transform infrared (FT-IR) and Raman measurements. The morphological features of composites are practically independent of subphase Zn concentration and are largely determined by the temperature of rapid thermal treatment. FT-IR results indicate the presence of zinc carboxylate in composites and HR-TEM results confirm the formation of ZnO nanoparticles upon subsequent oxidation. XPS and Raman measurements show that rapid thermal treatment in oxygen ambient results in decrease of carbon-oxygen functional groups and increase in graphitic carbon content leading to the reduction of GO in the composites. The average optical transmittance of rGO-ZnO composites in the visible region is found to be ∼87%. Photocatalytic studies carried out on methylene blue (MB) overlayer coated rGO-ZnO composites show reduction in concentration of MB with increasing duration of UV irradiation. The transparent two-dimensional rGO-ZnO composite solid state structures thus facilitate efficient adsorption and degradation of MB molecules, without any composite aggregation.

Near room temperature reduction of graphene oxide Langmuir-Blodgett monolayers by hydrogen plasma.

Langmuir-Blodgett monolayer sheets of graphene oxide (GO) were transferred onto Si and SiO2/Si, and subjected to hydrogen plasma treatment near room temperature. GO monolayers were morphologically stable at low power (15 W) plasma treatment, for durations up to 2 min and temperatures up to 120 °C. GO monolayers reduced under optimized plasma treatment conditions (30 s duration at 50 °C) exhibit a sheet thickness of (0.5-0.6) nm, high sp(2)-C content (75%), a low O/C ratio (0.16) and a significant red-shift of Raman G-mode to 1588 cm(-1), indicating efficient de-oxygenation and a substantial decrease of defects. A study of the valence band electronic structure of hydrogen plasma reduced GO monolayers shows an increase of DOS in the vicinity of the Fermi level, due to the increase of C 2p-π states, and a substantial decrease of work function. These results, along with conductivity measurements and transfer characteristics, reveal the p-type nature of hydrogen plasma reduced GO monolayers, displaying a conductivity of (0.2-31) S cm(-1) and a field effect mobility of (0.1-6) cm(2) V(-1) s(-1). Plasma treatment at higher temperatures results in a substantial increase in sp(3)-C/damaged alternant hydrocarbon content and incorporation of defects related to the hydrogenation of the graphitic network, as evidenced by multiple Raman features, including a large red-shift of D-mode to 1331 cm(-1) and a high I(D)/I(G) ratio, and supported by the appearance of mid-gap states in the vicinity of the Fermi level.

Growth of CdS nanocrystallites on graphene oxide Langmuir-Blodgett monolayers.

Large area GO-Cd composite Langmuir-Blodgett monolayers were transferred onto Si substrate by introducing Cd(2+) ions into the subphase. The changes in the behaviour of the Langmuir monolayer isotherm in the presence of Cd(2+) ions are attributed to changes in the microstructure and density of the GO sheets on the subphase surface. The uptake of Cd onto the GO monolayers and the effect of subsequent sulphidation were investigated by AFM, FTIR, Raman, XPS and HRTEM techniques. The incorporation of Cd into the GO monolayers causes some overlapping of sheets and extensive formation of wrinkles. Sulphidation of the GO-Cd sheets results in the formation of uniformly distributed CdS nanocrystallites on the entire basal plane of the GO monolayers. The de-bonding of Cd with oxygen functional groups results in a reduction of the wrinkles. The GO sheets function primarily as a platform for the interaction of metal ions with oxygen functionalities and their structure and characteristic features are not affected by either uptake of Cd or formation of CdS.