Reduced Graphene Oxide Research Articles

Impact of Dispersive Solvent and Temperature on Supercapacitor Performance of N-Doped Reduced Graphene Oxide

Impact of Dispersive Solvent and Temperature on Supercapacitor Performance of N-Doped Reduced Graphene Oxide

Ferroelectric Dipoles Tailoring Solid-Electrolyte-Interphase Chemistry to Enable Reversible Lithium Metal Batteries.

Solid-electrolyte interphase (SEI) plays a decisive role in building reliable Li metal batteries. However, the scarcity of anions in Helmholtz layer (HL) caused by electrostatic repulsion usually leads to the inferior SEI derived from solvents, resulting in dendrites and 'dead' Li. Therefore, regulating the distribution of anions in electric double layer (EDL) and continuously introducing more anions into HL to tailor anions-derived SEI is crucial for achieving stable Li plating/stripping. Herein, by jointly utilizing the controlled defects of reduced graphene oxide (rGO) and the oriented dipoles of ferroelectric BaTiO3 (BTO), the rGO-BTO composite layer sustainedly brings more TFSI- and NO3- into anion-defecient HL, promoting favorable decomposition of anions and guiding the generation of robust and fast-Li+-transport SEI containing more inorganics LiF and Li3N species. Thus, the resulting Li deposit shows smooth and dense morphologies without dendrites, leading to high average Coulombic efficiency. The Li//Cu@rGO-BTO (10 mAh cm-2 plated Li) cell exhibits an enhanced Li plating/stripping stability (2700 h) and a higher rate capability. The LiFePO4 full cell (N/P=~6.3) using rGO-BTO displays an enhanced capacity retention (82.0% @ 430 cycles). This work provides a new insight on the construction of robust SEI by regulating the distribution of anions within EDL.

3D Printed Ordered Hierarchically‐Porous Electrodes for Developing High‐Performance Quasi‐Solid‐State Aqueous Nickel‐Iron Batteries

AbstractStructural engineering offers a viable and broadly applicable approach for further enhancing the energy density of aqueous nickel‐iron (Ni‐Fe) batteries without changing the fundamental battery chemistries. Herein, the synthesis of 3D printed low‐tortuosity and ultra‐thick ordered hierarchically porous reduced graphene oxide (rGO)‐based microlattice electrodes for high‐performance aqueous Ni‐Fe batteries through direct writing (DIW) 3D printing technology is presented. Significantly, the areal specific capacitance of the 3D printed electrodes scales positively with electrode thickness, whereas the gravimetric capacitance remains relatively constant, indicating that the capacitive performance is not constrained by ion diffusion and exhibits rapid kinetic behavior, even at elevated mass‐loading levels and in the context of ultra‐thick electrodes. Based on a 3 m KOH aqueous electrolyte, the 3D printed aqueous Ni‐Fe cell (thickness: ≈2 mm) exhibits high areal specific capacity (≈0.353 mAh cm−2), high volumetric energy/power density (≈1.15 mWh cm−2 at 48.00 mW cm−2), and excellent long‐term cycling performance (≈81.25% capacitance retained after 5000 cycles). As a micro‐battery device, 3D printed quasi‐solid‐state Ni‐Fe battery (3DP QSS Ni‐Fe) device with 4 mm thickness still exhibits a high areal capacity of 0.525 mAh cm−2, and excellent cycle stability with ≈81.1% capacity retention after 10000 cycles. The promising 3D printed strategy provides a novel avenue for the controllable assembly of higher‐dimensional architectures, thereby paving the way for the advancement of next‐generation materials and devices.

The Construction of Face-to-Face Combination between NiFe-layered Double Hydroxide Nanosheets and Monolayer rGO for Efficient Water Splitting and Oxygen Reduction.

Developing cost-effective and efficient electrocatalysts is essential for advancing a green energy future. Herein, a NiFe-layered double hydroxide loaded on reduced graphene oxide (NiFe-LDHs@rGO) hybrid was synthesized using a straightforward three-step process involving exfoliation tearing, electrostatic self-assembly, and chemical reduction. The face-to-face packing and ultrathin exfoliation enable strong heterogeneous interactions, fully harnessing the potential of these complementary two-dimensional counterparts. Consequently, the resultant catalyst displays outstanding oxygen evolution reaction (OER) catalytic activity and stability, whose overpotential is as low as 241 mV at 30 mA cm-2 and 255 mV at 50 mA cm-2 with a low Tafel slope of 62.1 mV dec-1. Both the experimental results and density functional theory (DFT) calculations reveal that the face-to-face assembly strengthens the electronic interactions between NiFe-LDHs and rGO, which effectively modulates the d-band center of Ni and Fesites and improves the reaction kinetics for OER. Moreover, the resultant NiFe-LDHs@rGO hybrids exhibit excellent multifunctional catalytic performance. Its hydrogen evolution reaction (HER) activity is endowed by Fe-site of NiFe-LDHs and defect states rGO and achieves a low voltage of 1.68 V to drive a current density of 10 mA cm-2 for overall water splitting. The face-to-face heteroassembly also imparts NiFe-LDHs@rGO with superior oxygen reduction reaction (ORR) activity, with a half-wave potential of 0.70 V and a limiting current density of 4.2 mA cm-2. Its ORR primarily follows a four-electron transfer pathway with a minor contribution from a two-electron process. This study establishes the groundwork for optimizing two-dimensional heterogeneous interfaces in LDH@carbon-based materials for advanced energy conversion.

Numerical investigation of graphene derivatives as HTL in PBDB-T:NCBDT bulk heterojunction organic solar cell

The damaging effects of the most widely used PEDOT:PSS have led researchers to search for an alternative hole transport layer (HTL) in non-fullerene acceptor (NFA) based bulk heterojunction organic solar cells (BHJOSC’s). This work highlights the numerical simulation study of possible new approach of utilizing graphene, graphene oxide (GO), reduced graphene oxide (rGO), and p type doped graphene (p-graphene), as an alternative to PEDOT:PSS in non-fullerene acceptor based bulk heterojunction organic solar cell (NFABHJOSC) with PBDB-T as donor and NCBDT as acceptor using SCAPS1D. NCBDT is an emerging small-molecule non-fullerene acceptor (SM-NFA) whose bandgap can be tuned and reduced, making it a better option as an acceptor. Validation of the software is done by matching simulation results with experimental results. Diverse electron transport layers (ETL’s), including PDINO, ZnO, IGZO, TiO2, TiO2:gr (20%) composite, and TiO2:gr (10%) composite, are introduced, and device performance of various configurations is analysed. Optimization of the best device configuration ITO (4.8 eV)/rGO/PBDB-T:NCBDT/PDINO/Al gave an improved efficiency of 17.47%, fill factor (FF) of 77.45%, short circuit current density (Jsc) of 25.407 mA/cm2, and an open circuit voltage (Voc) of 0.8878 V.

Efficient photocatalytic degradation of chloramphenicol from contaminated water over rGO@MoS2 nanocomposites

Antibiotics-based effluents pose a severe threat to the natural ecosystem by acting as reservoirs for the growth of drug-resistant bacteria if untreated. Herein, a facile and scalable approach was developed to engineer photocatalysts associating reduced graphene oxide (rGO) and molybdenum disulfide (rGO@MoS2) that were used for the degradation of chloramphenicol (CAP) from contaminated water under UV-light. The hydrothermally produced rGO@MoS2 catalysts contain CO, COH, and COC functional groups that contribute to the binding of CAP onto their surface. The rGO surface modification with MoS2 layers offers a high surface area for light absorption. Results show that the rGO@MoS2 catalyst (1:1 w/w) exhibits the highest degradation efficiency (DE) of 86 % within 180 min of light exposure at neutral pH. Further, the kinetic modelling studies for CAP degradation by rGO@MoS2 1:1 showed high linearity with pseudo-first order kinetics (R2 ∼ 0.9). The isotherm modelling studies correspond to Langmuir isotherm (R2 ∼ 0.99), suggesting monolayer-type interaction of CAP with the photocatalyst surface during photodegradation. Furthermore, the mechanism of degradation elucidated using scavenging experiments showed the involvement of both holes (h+) and electrons (e−) that contribute to the degradation of CAP by generating reactive oxygen species (ROS) like OH● and O2●− radicals. The applicability of the rGO@MoS2 photocatalyst towards the degradation of CAP was tested in Ganga water, wherein a similar ∼86 % CAP removal was observed. Furthermore, the photocatalyst was found to be stable and could be reused five times. Overall, these findings demonstrate the usefulness of the rGO@MoS2 1:1 composite as an efficient photocatalyst that can be used for the degradation of harmful organic pollutants from water bodies to provide a safer and cleaner environment.

Ce-doped NiCo-layered double hydroxide based self-supporting tremella-shaped nanoflower heterostructure as efficient electrocatalyst for the oxygen evolution reaction

NiCo-layered double hydroxide (NiCo-LDH) catalysts, which indicate a profound prospect of oxygen evolution reaction (OER) under alkaline conditions, are facing great challenges in terms of low electrical conductivity, restricted by poor conductivity, limited electrochemical reaction sites, and low-density of edge sites. The authors developed a simple and convenient in-situ one-pot self-assembly method. The Ce-doped defective NiCo-LDH hexagonal nanosheets and nitrogen-doped graphene fabricated the NiCoCe-LDH/RNF electrocatalyst on the nickel foam (NF) substrate, which demonstrated excellent OER activity under alkaline conditions, only needed 299 mV overvoltage to achieve 50 mA cm−2 current intensity, could last for 6 hours at 20 mA cm−2. The highly active OER benefited from the structural advantages of the novelty three-dimensional array structure. The novel geometric structure of tremella-shaped nanoflower integrated with curved nanosheets and curled edges loaded on NF provides more electrochemical reaction sites for intermediate coordination. The nitrogen-doped reduced graphene oxide accommodated better interaction between active materials and charge carriers, enhancing the conductivity and electron transfer performance of nanostructures. The effective synergistic between the heterostructures promoted the excellent OER electrocatalytic activity of NiFeCe-LDH/RNF nanocomposites. DFT calculations at the atomic level of pristine and Ce-doped NiCo-LDH exhibited that Ce-doping can reduce the Gibbs free energy of the potential-determining step and improve the catalytic activity of OER. This work has broadened the horizons for developing simple and highly available OER electrocatalysts.

Self-powered, highly selective and fast response time ammonia gas sensors based on an rGO/SnO2 nanocomposite

Improving the sensitivity and selectivity of ammonia gas sensors at room temperature is essential for the development of self-powered sensors to expand their operational range in various environments. The strategy employed in this study to achieve this goal involves combining reduced graphene oxide (rGO), known for its excellent electrical properties, with SnO2, which has been reported to have ammonia-sensing capabilities. For this purpose, the rGO-SnO2 nanocomposite was synthesized using a two-step pyrolysis and chemical deposition method, and its ammonia gas sensing performance was evaluated. Structural characterization of the synthesized sample was conducted using XRD, BET, SEM, PL, EDX and FTIR techniques. The sensor's response to different concentrations of ammonia gas at room temperature was investigated, and the results showed a 5.2% response at 800 ppm and a low detection limit of 1.43 ppm for this gas. In addition to its high selectivity for ammonia gas, the sensor also demonstrated stability and repeatability.

Soil Potassium Sensor Using a Valinomycin-Decorated Reduced Graphene Oxide (rGO-v)-Based Field-Effect Transistor for Precision Farming

Soil Potassium Sensor Using a Valinomycin-Decorated Reduced Graphene Oxide (rGO-v)-Based Field-Effect Transistor for Precision Farming

Genipin Nanoparticles-Doped Reduced Graphene Oxide Membranes: A Promising Solution for Arsenic Ion Removal From Wastewater

Genipin Nanoparticles-Doped Reduced Graphene Oxide Membranes: A Promising Solution for Arsenic Ion Removal From Wastewater

ZnS and Reduced Graphene Oxide Nanocomposite-Based Non-Enzymatic Biosensor for the Photoelectrochemical Detection of Uric Acid.

In this work, we report a study of a zinc sulfide (ZnS) nanocrystal and reduced graphene oxide (RGO) nanocomposite-based non-enzymatic uric acid biosensor. ZnS nanocrystals with different morphologies were synthesized through a hydrothermal method, and both pure nanocrystals and related ZnS/RGO were characterized with SEM, XRD and an absorption spectrum and resistance test. It was found that compared to ZnS nanoparticles, the ZnS nanoflakes had stronger UV light absorption ability at the wavelength of 280 nm of UV light. The RGO significantly enhanced the electron transfer efficiency of the ZnS nanoflakes, which further led to a better photoelectrochemical property of the ZnS/RGO nanocomposites. The ZnS nanoflake/RGO nanocomposite-based biosensor showed an excellent uric acid detecting sensitivity of 534.5 μA·cm-2·mM-1 in the linear range of 0.01 to 2 mM and a detection limit of 0.048 μM. These results will help to improve non-enzymatic biosensor properties for the rapid and accurate clinical detection of uric acid.

Quantification of the Contribution of Heterogeneous Surface Processes to Pollutant Abatement during Heterogeneous Catalytic Ozonation.

Heterogeneous surface processes such as adsorption and oxidation with surface-adsorbed reactive oxygen species (ROSad, e.g., adsorbed oxygen atom (*Oad) and hydroxyl radicals (•OHad)) have been suggested to play an important role in pollutant abatement during heterogeneous catalytic ozonation (HCO). However, to date, there is no reliable method to quantitatively evaluate the contribution of heterogeneous surface processes to pollutant abatement (fS) during HCO. In this study, we developed a method by combining probe compound-based experiments with kinetic modeling to distinguish heterogeneous surface processes from homogeneous bulk reactions with aqueous O3 and ROS (•OH and superoxide radicals (O2•-) in the abatement of various pollutants (e.g., atrazine, ibuprofen, tetrachloroethylene, and perfluorooctanoic acid) during HCO with reduced graphene oxide. The results show that the pollutants that have a low affinity for the rGO surface (e.g., ibuprofen and tetrachloroethylene) were essentially abated by homogeneous bulk reactions, while the contribution of heterogeneous surface processes was negligible (fS < 5%). In contrast, heterogeneous surface processes played an important or even dominant role in the abatement of pollutants that have a high surface affinity (e.g., fS = 32-82% for atrazine and perfluorooctanoic acid). This study is a critical first step in quantitatively evaluating the role of heterogeneous surface processes for pollutant abatement during HCO, which is crucial to understanding the mechanism of HCO and designing catalysts for effective pollutant abatement.

Solar driven highly efficient photocatalyst based on Dy2O3 nanorods deposited on reduced graphene oxide nanocomposite for methylene blue dye degradation.

In recent years, the demand for rare earth elements has surged due to their unique characteristics and diverse applications. This investigation focuses on utilizing the rare earth element dysprosium oxide (Dy2O3) for the photocatalytic oxidation of model pollutants under solar light irradiation. A novel RGO-Dy2O3 nanocomposite photocatalyst was developed using a solvothermal approach, Dy2O3 nanorods uniformly deposited onto reduced graphene oxide (RGO) nanosheets. Comprehensive characterization techniques, including Brunner-Emmett-Teller (BET), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), Fourier transform-infrared spectroscopy (FTIR), Raman spectroscopy, high resolution - transmittance electron microscopy (HR-TEM), field emission-electron scanning microscopy (FE-SEM), atomic force microscopy (AFM), electron paramagnetic resonance spectroscopy (EPR), photoluminescence spectroscopy (PL), and electrochemical impedance spectroscopy EIS techniques. The UV-visible diffusive reflectance spectroscopy (UV-Vis-DRS) studies revealed a band gap energy of 3.18eV and a specific surface area of 114 m2/g for the fabricated RGO-Dy2O3 nanocomposite. The RGO-Dy2O3 nanocomposite demonstrated a high photocatalytic degradation efficiency of 98.1% at neutral pH for methylene blue (MB) dye for the dye concentration of 10ppm. The remarkable photocatalytic performance was achieved within 60min under solar light irradiation. Reusability tests demonstrated stability, maintaining over 90% photocatalytic efficiency after three cycles. The EPR spectra and quenching experiments confirmed that photogenerated hydroxyl radicals significantly influence the photodegradation processes. The RGO-Dy2O3 nanocomposite photocatalyst, with its green, easy preparation process and recycling capabilities, presents an ideal choice for various applications. It offers a viable alternative for the photocatalytic degradation of organic dyes in real wastewater, contributing to sustainable environmental remediation.

Negative Effect of the Calendering Process on the Interphase Formation and Electrochemical Behavior of Reduced Graphene Oxide Electrodes.

Many studies on electrode material development for rechargeable batteries have focused on improving the intrinsic physicochemical and electrochemical properties of active materials, but the electrochemical performances of batteries are exhibited by the overall electrode unit consisting of active materials, conductive additives, and a binder. Additionally, the electrodes have undergone an essential calendering process to enhance the physical contact between those components. Therefore, the electrochemical behavior and performance of a cell should be analyzed at the electrode level, as the inherent properties of active materials might be changed in electrode preparation, including the calendaring process and real-operating environments. In this study, we aimed to understand the electrochemical properties of the reduced graphene oxide (RGO)-containing electrodes rather than the RGO-active materials by studying the changes in the RGO electrode before and after the calendering process. Specifically, the study investigates the effect of the calendering process on the electrochemically active interphase formation and electrochemical properties of the RGO electrode. We found that the calendering process deteriorates the electrochemical properties of RGO electrodes by impeding enough electrolyte wetting, limiting the formation of thin and stable solid-electrolyte interphase, and leaving unreacted RGO sheets. Additional experiments with carbon-coated silicon/RGO composite electrodes demonstrate that after the calendering process, the sequential participation of Si/C particles in the electrochemical reaction resulted in much more severe capacity degradation over repeated cycling processes. The studies suggest that fine-controlling the number of RGO sheets and maintaining enough distance between those sheets even after the calendering process are required for the utilization of RGO in rechargeable batteries.

A Direct Current Self-Sustained Moisture-Electric Generator with 1D/2D Hierarchical Nanostructure for Continuous Operation of Off-Grid Electronics.

Ubiquitous moisture is a colossal reservoir of clean energy, and the emergence of moisture-electric generators (MEGs) is expected to provide direct power support for off-grid electronic devices anytime and anywhere. However, most MEGs rely on auxiliary energy storage devices and rectifier circuits to drive small electronic devices, which hinder scalability and widespread deployment, and the development of direct current (DC) MEGs with high power output that can directly drive off-grid electronic devices is highly promising but challenging. Herein, a self-sustained moisture-electric generator (SMEG) with a hierarchical nanostructure based on one-dimensional (1D) negatively charged nanofibers and two-dimensional (2D) conductive nanosheets was demonstrated to generate continuous DC electricity from atmospheric humidity. Sulfation of bacterial cellulose nanofibers lowers the surface potential and increases the surface charge energy, and reduced graphene oxide (rGO) provides a conduction pathway for electrons. The hierarchical nanostructures constructed by the combination of 1D nanofibers and 2D nanosheets endow the SMEG with self-sustained moisture gradients and structural anisotropy, which force the generation of a pseudocurrent. This combination also constructs microcapacitors that further enhance the moisture-electric power output. The SMEG can generate a continuous voltage in excess of 0.54 V for over 2160 h, with a power density of about 822 μW cm-3, demonstrating excellent operational durability. This research provides a feasible solution for the development of sustainable, versatile, and efficient power supplies for off-grid self-powered devices.

Hierarchical Engineering on Built‐In Electric Field of Bimetallic Zeolitic Imidazolate Derivatives Towards Amplified Dielectric Loss

AbstractConstruction of built‐in electric field (BIEF) in nanohybrids has been demonstrated as an efficacious strategy to boost the dielectric loss by facilitating oriented transfer and transition of charges, thus optimizing the electromagnetic wave absorption property. However, the specific influence of BIEF on interface polarization needs to explore thoroughly and the BIEF strength should be further augmented. Herein, several dielectric systems incorporated Mott–Schottky heterojunctions and hollow structures are designed and constructed, where bimetallic zeolitic imidazolate framework are employed to derive Cu‐ZnO Mott–Schottky heterojunctions, and hierarchical structures and BIEF are further enriched by introducing hollow structure and reduced graphene oxide. The well‐established “double” BIEF verified by theoretical calculation and hollow engineering can regulate the conductivity, and enhance the polarization relaxation effectively. Especially, there always coexisted both enhanced charge separation and reversed charge distribution in this “double” BIEF, boosting the interface polarization. Attributing to the synergy of well‐matched impedance and amplified dielectric loss, the obtained hybrids exhibited superior absorption (reflection loss of −46.29 dB and an ultra‐wide effective absorption bandwidth of 7.6 GHz at only 1.6 mm). This work proves an innovative model for dissecting dielectric loss mechanisms and pioneers a novel strategy to explore advanced absorbers through enhancing BIEF.

Advancement of Electro-Optical Properties through Changes in the Physicochemical Composition of Hybrid Thin Films by Doping Reduced Graphene Oxide into a Sol-Gel Process Solution.

A hybrid thin film was fabricated by doping graphene oxide into a sol-gel solution containing a mixture of zirconium, bismuth, and indium oxide. The thin film was fabricated using a brush coating process. The graphene oxide doping ratios used were 0, 5, and 15 wt%. During the thin film fabrication process, the produced sol-gel solution generates a contractile force due to the shear stress of the brush bristles, resulting in a microgroove structure. This structure was confirmed through scanning electron microscopy analysis, which revealed the clear presence of rGO. Comparing the electrical properties of a zirconium bismuth indium oxide thin film without graphene oxide doping and a thin film doped with 15 wt% graphene oxide, the electro-optical properties were significantly improved with graphene oxide doping. In general, the threshold voltage decreased by approximately 0.42 V. In addition, bandgap measurements confirmed the improved conductivity characteristics with graphene oxide doping. Since this improvement in electro-optical properties is associated with the reduction process due to graphene oxide doping, X-ray photoelectron spectroscopy analysis was performed to assess the intensity change of each element. Based on these observations, hybrid thin films doped with graphene oxide emerge as promising candidates for next generation thin film.

Fluorinated reduced graphene oxide nanosheets for symmetric supercapacitor device performance

This study explores the potential of using spent lithium-ion battery anodes (graphite) for fabricating symmetric energy devices through a simple regeneration process. Specifically, the use of fluorine-doped reduced graphene oxide (RGO) nanosheets derived from waste batteries as the basis for a symmetric supercapacitor (SC) device is investigated. To enhance the electrochemical energy storage capabilities, a facile hydrothermal technique is employed to synthesize fluorinated graphene. Fluorination of the graphene sheets is successfully realized, as confirmed by the presence of boron with a 2.94 at.% fluorine-doped level, according to the Energy dispersive spectroscopy (EDS) spectrum analysis. Electrochemical analysis of the F-RGO electrode performance consistent with electric double-layer capacitance. Moreover, with a three-electrode system, the F-RGO electrode achieves a maximum specific capacitance of 207F/g under a current density of 1 A/g. A two-electrode symmetric device employing F-RGO exhibits a specific capacitance of 54F/g at 1 A/g. Furthermore, electrochemical impedance measurements demonstrate low charge transfer resistance (Rct) values, specifically 8.63 Ω for F-RGO, signifying improved electrochemical performance. Thus, fluorine atomic doping in RGO nanosheets contributes to the improvements of the specific capacitance and overall superior electrochemical performance of F-RGO, and F-RGO is a highly electrochemical active material for high-performance energy storage electrodes for SCs.

A multifunctional biomass-based solar interface evaporator with feather-like structure for efficient selective transport, antibacterial properties, salt resistance, and oil-fouling prevention

Solar interface evaporation technology has gained prominence as an efficient, low-cost, and CO2-neutral method for water purification. However, the development of interface evaporators with high evaporation efficiency, durability, and environmentally friendly, cost-effective materials remains a significant challenge. In this study, we fabricated a novel solar-powered hydrogel membrane using sodium alginate (SA), reduced graphene oxide (RGO), and vegetable-tanned collagen fibers (CF). Utilizing a dual-structural engineering design strategy, which incorporates surface patterning and microfiber channel construction, the resulting sodium alginate/collagen fibers/reduced graphene oxide (CF/SA/RGO) composite membranes exhibited remarkable selective mass transport efficiency. The inclusion of vegetable-tanned collagen fibers notably enhanced the flow rate of free water within the CF/SA/RGO membranes. Moreover, the reduction in water evaporation enthalpy increased with successive GO reduction cycles, thereby further boosting the evaporation rate. The CF/SA/RGO membranes demonstrated an outstanding evaporation efficiency of 2.88 kg m−2 h−1, ion rejection rates of 98 % for K+, Ca2+, Na+, and Mg2+, and a dye removal efficiency of 99.52 % for RhB, MB, MO, and CR. Additionally, these membranes exhibited excellent underwater oleophobicity, antibacterial properties, and salt resistance. This study offers a novel approach to the design and fabrication of solar interface evaporators, presenting an advancement in achieving high solar energy conversion efficiency and superior operational durability.

Compositing of rGO to TiO2 by Low-Temperature Treatment and Their Photocatalytic Properties

Reduced graphene oxide (rGO)/TiO2 nanocomposites were prepared by low-temperature and low-pressure heat treatment. The structure and photocatalysis performance of the composites were characterized by transmission electron microscopy (TEM), Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), and UV-visible diffuse reflectance spectrum (UV-Vis DRS). The photocatalytic degradation performance of methyl orange (MO) by composites with different raw material ratios was studied under simulated solar-irradiation conditions. Results indicated that graphene oxide (GO) was reduced to graphene during heat treatment and bonded well with TiO2. Compared with TiO2, GO addition greatly improved its photocatalytic efficiency. Under simulated sunlight irradiation, the samples exhibited good photocatalysis performance. Within 50[Formula: see text]min, MO can be rapidly degraded by TiO2/40% rGO composite.