Surface modified and functionalized graphene oxide membranes for separation of strontium from aqueous solutions.

Graphene oxide-strontium (GO-Sr) composites prepared under different ambient conditions were characterized using morphological and spectroscopic techniques to optimize the uptake of Sr from aqueous solutions. These studies indicated that interactions among GO and Sr2+ ions are highly sensitive to size and aging of GO sheets, as well as pH of the ambience. Further, the extent of Sr uptake on GO sheets was found to be largely influenced by relative fractions of the associated -COOH, -OH, C-O-C functional groups and sp2-C domains. Membranes prepared using various forms of GO were evaluated for their Sr separation ability and, a window of parameters for optimum separation of Sr has been proposed. Among the variety of membranes studied, those made up of fresh and large GO sheets were found to exhibit superior Sr adsorption capacity (~296 mg/g) at limited GO mass. Further, adsorption efficiency of these GO membranes was observed to deteriorate with aging of GO sheets and rise of GO mass on membrane. The membrane based filtration procedure introduced in present work facilitates to provide a lamellar structure of GO sheets with abundant surface area, diverse and accessible sites for Sr2+ ion uptake and offer high Sr adsorption efficiencies.

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.

Study of simultaneous reduction and nitrogen doping of graphene oxide Langmuir-Blodgett monolayer sheets by ammonia plasma treatment.

Graphene oxide (GO) monolayer sheets, transferred onto Si by the Langmuir-Blodgett technique, were subjected to ammonia plasma treatment at room temperature with the objective of simultaneous reduction and doping. Scanning electron microscopy and atomic force microscopy studies show that plasma treatment at a relatively low power (∼10 W) for up to 15 min does not affect the morphological stability and monolayer character of GO sheets. X-ray photoelectron spectroscopy has been used to study de-oxygenation of GO monolayers and the incorporation of nitrogen in graphitic-N, pyrrolic-N and pyridinic-N forms due to the plasma treatment. The corresponding changes in the valence band electronic structure, density of states at the Fermi level and work function have been investigated by ultraviolet photoelectron spectroscopy. These studies, supported by Raman spectroscopy and electrical conductivity measurements, have shown that a short duration plasma treatment of up to 5 min results in an increase of sp²-C content along with a substantial incorporation of the graphitic-N form, leading to the formation of n-type reduced GO. Prolonged plasma treatment for longer durations results in a decrease of electrical conductivity, which is accompanied by a substantial decrease of sp²-C and an increase in defects and disorder, primarily attributed to the increase in pyridinic-N content.

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.