Toward Green Synthesis of Graphene Oxide Using Recycled Sulfuric Acid via Couette-Taylor Flow

Developing eco-friendly and cost-effective processes for the synthesis of graphene oxide (GO) is essential for its widespread industrial applications. In this work, we propose a green synthesis technique for GO production using recycled sulfuric acid and filter-processed oxidized natural graphite obtained from a Couette-Taylor flow reactor. The viscosity of reactant mixtures processed from Couette-Taylor flow was considerably lower (???200 cP at 25 ??C) than that of those from Hummers' method, which enabled the simple filtration process. The filtered sulfuric acid can be recycled and reused for the repetitive GO synthesis with negligible differences in the as-synthesized GO qualities. This removal of sulfuric acid has great potential in lowering the overall GO production cost as the amount of water required during the fabrication process, which takes a great portion of the total production cost, can be dramatically reduced after such acid filtration. The proposed eco-friendly GO fabrication process is expected to promote the commercial application of graphene materials into industry shortly

Impedance Spectroscopy Analysis and Equivalent Circuit Modeling of Graphene Oxide Solutions

The optical and electrical characteristics of a graphene oxide solution (GS) with different graphene oxide (GO) concentrations in de-ionized water are investigated via the electrochemical impedance spectroscopy (EIS) method. The measurement results produced by the EIS for the GS are represented with both Bode and Nyquist plots in a frequency range from 1 kHz to 10 MHz. Using these results, we develop an equivalent circuit model as a function of the GO concentration, representing the GS as a mixed circuit of two-dimensional (2D) GO dispersed in parallel in de-ionized (DI) water. The underlying physics of the current-flowing behavior in the GS are explained and interpreted using empirical circuit models; the circuit model also shows that highly resistive GO becomes conductive in GS form in the DI water. The findings in this work should draw new attention toward GSes and related applications, including functional composite materials, catalysts, and filter membranes

Compliment Graphene Oxide Coating on Silk Fiber Surface via Electrostatic Force for Capacitive Humidity Sensor Applications

Cylindrical silk fiber (SF) was coated with Graphene oxide (GO) for capacitive humidity sensor applications. Negatively charged GO in the solution was attracted to the positively charged SF surface via electrostatic force without any help from adhesive intermediates. The magnitude of the positively charged SF surface was controlled through the static electricity charges created on the SF surface. The GO coating ability on the SF improved as the SF’s positive charge increased. The GO-coated SFs at various conditions were characterized using an optical microscope, scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), Raman spectroscopy, and LCR meter. Unlike the intact SF, the GO-coated SF showed clear response-recovery behavior and well-behaved repeatability when it was exposed to 20% relative humidity (RH) and 90% RH alternatively in a capacitive mode. This approach allows humidity sensors to take advantage of GO’s excellent sensing properties and SF’s flexibility, expediting the production of flexible, low power consumption devices at relatively low costs

A Gallium Oxide-Graphene Oxide Hybrid Composite for Enhanced Photocatalytic Reaction

Hybrid composites (HCs) made up of gallium oxide (GaO) and graphene oxide (GO) were investigated with the intent of enhancing a photocatalytic reaction under ultraviolet (UV) radiation. The material properties of both GaO and GO were preserved, even after the formation of the HCs. The incorporation of the GO into the GaO significantly enhanced the photocatalytic reaction, as indicated by the amount of methylene blue (MB) degradation. The improvements in the reaction were discussed in terms of increased surface area and the retarded recombination of generated charged carriers

Enhanced Photocatalytic Degradation of 2-Butanone Using Hybrid Nanostructures of Gallium Oxide and Reduced Graphene Oxide Under Ultraviolet-C Irradiation

Hybrid nanostructures made of gallium oxide (Ga2O3) and reduced graphene oxide (rGO) are synthesized using a facile hydrothermal process method, where the Ga2O3 nanostructures are well dispersed on the rGO surface. The formed Ga2O3-rGO hybrids are characterized via Field emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), a diffuse reflectance Ultraviolet-visible-near infrared (UV-Vis-NIR) spectrophotometer, Brunauer–Emmett–Teller (BET), and photoluminescence (PL). Gas chromatography mass spectrometry (GC-MS) was used for analyzing volatile organic compounds (VOCs). The photocatalytic activity of the hybrid nanostructures is evaluated via the degradation of the 2-butanone, representing the VOCs under 254-nm radiation in the atmosphere. That activity is then compared to that of the Ga2O3 and commercial TiO2-P25. The Ga2O3-rGO hybrid shows enhanced photocatalytic degradation of 2-butanone compared to Ga2O3 and TiO2-P25, which is attributed to the enhanced specific surface area. The results indicate that the Ga2O3-rGO hybrid could be a promising method of enhancing photocatalytic activity and thereby effectively degrading VOCs, including the 2-butanone

A Zero-Power, Low-Cost Ultraviolet-C Colorimetric Sensor Using a Gallium Oxide and Reduced Graphene Oxide Hybrid via Photoelectrochemical Reactions

A zero-power, low-cost ultraviolet (UV)-C colorimetric sensor is demonstrated using a gallium oxide and reduced graphene oxide (rGO) hybrid via photoelectrochemical reactions. A wide bandgap semiconductor (WBS) such as gallium oxide with an energy bandgap of 4.9 eV generates electron-hole pairs (EHPs) when exposed under a mercury lamp emitting 254 nm. While the conventional UVC sensors employing WBS convert the generated EHPs into an electrical signal via a solid-state junction device (SSD), our newly proposed UVC sensory system works by converting EHPs into an electrochemical reaction. The electrochemical reaction causes the degradation of a cationic thiazine redox dye, methylene blue (MB) and thereby spontaneously changes its color. As more rGO was hybridized with the gallium oxide, MB degradation was effectively expedited. Thus, the level of MB degradation under UVC can be evaluated as a UVC indicator. Unlike conventional SSD-based UVC sensors, our responsive colorimetric sensor can be applied where needed inexpensively and zero power