GO Layers Research Articles

ZIF-67 derivatives of NiCo2S4 Decorated in Salen-Complex Amine Functionalization GO Layers for High-Performance Applications in Supercapacitor Devices.

The study develops polyamine-functionalized graphene oxide-supported NiCo2S4 nanomaterial using a metal-organic framework (MOF). This modification adds free amines and oxygen functionality to the graphene oxide electrode surface, resulting in the decrease in the 2 theta value from 11.2 to 7.1 and an increase in the interlayer spacing value from 1.4 to 7.8 nm. This modification enhances the surface properties, leading to improved wettability and dispersion stability. Additionally, bimetallic nanoparticles of NiCo2S4, synthesized via the ZIF-67 MOF template, further enhance performance. Analysis confirms the successful fabrication of ZIF-67/f-GO/NiCo2S4 electrode material through various techniques such as XPS spectra, FE-SEM, XRD, and Raman spectra. The resulting Salen-fGO@NiCo2S4 composite exhibits impressive specific capacitance, reaching 2581.65 F g-1 at 10 A g-1 with 82% capacity retention after 5000 cycles. Employing this composite in a hybrid supercapacitor yields remarkable energy and power densities of 40 and 920 W kg-1, individually, while maintaining 74% capacity retention rate at 10 A g-1. These findings offer promising prospects for advanced energy storage applications.

Photocatalytic removal of aldrin and dieldrin using graphene oxide and TiO2‐doped CuFe2O4

AbstractBACKGROUNDConventional treatment processes and existing photocatalysts have proven insufficient in efficiently removing aldrin and dieldrin. Consequently, this study aimed to investigate the removal of aldrin and dieldrin from surface water using a titanium dioxide/graphene oxide/copper ferrite (TiO₂/GO/CuFe₂O₄) nanocomposite.RESULTSThe highest photodegradation efficiencies for aldrin (100%) and dieldrin (99%) were achieved with a TiO₂/GO/CuFe₂O₄ nanocomposite dosage of 1.3 mg L−1, at a sunlight intensity of 9 W m−2 and an optimal photodegradation time of 25 min. The maximum UV absorption wavelength of the TiO₂/GO/CuFe₂O₄ nanocomposite was observed at 365 nm. The quantum yield of the nanocomposite was recorded as 2.69 × 102 mol einstein−1, and its bandgap energy was determined to be 3.31 eV. The first‐order kinetic rate constants for aldrin and dieldrin were calculated as 0.05 and 0.047 min−1, respectively. X‐ray diffraction analysis confirmed the crystal structure of CuFe₂O₄/TiO₂, while Fourier transform infrared spectroscopy detected carboxylic, epoxy, carbonyl and other oxygenated groups within the TiO₂/GO/CuFe₂O₄ nanocomposite. Scanning electron microscopy and transmission electron microscopy images revealed that CuFe₂O₄ was situated on the outer layer of GO. Energy‐dispersive X‐ray analysis identified the elemental composition of the TiO₂/GO/CuFe₂O₄ nanocomposite as comprising GO, C, Cu, Fe, Ti and O. A reusability study demonstrated that the nanocomposite maintained excellent performance, achieving 99% removal efficiency after 79 cycles and 97% after 100 cycles.CONCLUSIONSThe TiO₂/GO/CuFe₂O₄ nanocomposite effectively removed aldrin and dieldrin from surface water. This nanocomposite holds promise for the remediation of other aquatic ecosystems, such as bays, rivers and ocean waters. © 2024 The Author(s). Journal of Chemical Technology and Biotechnology published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry (SCI).

In-situ exfoliating graphene to anchor Mo2C NPs and modulate crystal planes for hydrogen production

An economical and efficient noble metal-free catalyst is necessary for large-scale hydrogen production. Here, Mo2C nanoparticles (NPs) were well-dispersed on the surface of 2D graphene nanosheets by in-situ propping oxide graphene (GO) layers, anchoring molybdate ions between GO layers and pyrolysis. The exposed crystal planes were also adjusted by above strategy. The results indicate that uniform and well-dispersed Mo2C NPs with a narrow size distribution were anchored on 2D rGO nanosheets and exposed dual crystal planes. The results of hydrogen evolution reaction (HER) show that the optimal Mo2C/rGO catalyst only needs low overpotential (η10, 112 mV) to drive 10 mA cm−2 in alkaline solution, and η10 only increased by 12 mV after 1000 cycles test, indicating high activity and stability for HER. Notably, the overpotential is below than that of Pt/C commercial catalyst when current density is more than 100 mA cm−1. The excellent performance is benefit from low hydrogen adsorption Gibbs free energy (ΔGH∗) on the Mo2C catalyst. Therefore, the proposed strategy is efficient to prepare well-dispersed and dual crystal planes-exposed Mo2C NPs for electrocatalytic hydrogen evolution.

Enhanced water permeability and antifouling properties of cross-linked graphene oxide composite membranes with tunable d-spacings

Low flux and membrane fouling are major challenges in membrane distillation (MD) for treating concentrated wastewater. This study compared the performance of GO composite membranes with different interlayer distances, by covalently bonding the terminal amine groups of ethylenediamine (EDA) and 1,12-diaminododecane (DADD) with the carboxyl groups present on the GO sheets. The results indicated that the GO-DADD/PTFE membrane, with longer carbon chain cross-linking, achieved the highest flux and antifouling properties. At 70 °C, the pure water flux reached 68.5 kg/m2·h, and the fluxes for treating NaCl, HA containing NaCl, and BSA containing NaCl were 29.8 %, 37.1 %, and 38.5 % higher than the uncrosslinked GO/PTFE, and 95.7 %, 121.2 %, and 146.9 % higher than the PTFE membrane, respectively. Through mathematical models for mass and heat transfer, the study identified the key to this enhancement as the increased d-spacing within the GO layer due to cross-linking, which weakened the Kelvin effect and enhanced the vapor partial pressure on the hot side. The unique surface structure and electrostatic interactions induced by long-chain cross-linking further boosted the antifouling effect. These modifications not only overcome the typical trade-off between retention rates and flux but also offer a scalable and efficient solution for advanced membrane distillation applications.

Tuning optical, magnetic, and electrical parameters of CuFe2O4 nanoparticles incorporated with GO and ZnO using a facile synthesis

Nano-ferrites, metal oxides, and carbon-based nanomaterials have been used frequently to enhance optical and magnetic prospects for latent applications. Copper ferrite/Graphene Oxide and Zinc Oxide (CuFe2O4/GO/ZnO) ternary nanocomposite synthesized by hydrothermal route showed dramatically good outcomes as the band gap energy value of synthesized nanocomposite approaches to 2.4 eV. Furthermore, the light absorbance of CuFe2O4 increases by adding ZnO and GO. The experimental data revealed the face-centered cubic structure (FCC) of pure spinal ferrite (CuFe2O4) nanoparticles even after adding ZnO and GO. The 2θ peak observed at 31.70° with (220) hkl planes indicates the successful addition of ZnO nanoparticles in CuFe2O4/GO nanocomposite. XRD graph, the absence of characteristic peaks of GO revealed the intercalation of CuFe2O4 nanoparticles with GO layers. In SEM images, agglomeration among CuFe2O4 nanoparticles is observed due to the magnetic interaction of nano-crystallite with a high surface-to-volume (S/V) ratio. VSM can be used to determine the magnetic properties of as-synthesized samples at moderate temperatures under 0–0.5 and ± 5 tesla. In CuFe2O4/GO/ZnO ternary nanocomposite, the saturation magnetization value reduces from 2.071 to 1.365 emu/g due to the addition of ZnO nanoparticles. The loops were narrowed showing a decrease in the coercive field with the addition of ZnO nanoparticles in CuFe2O4/GO ternary nanocomposite material. Moreover, the study of electrical properties of pure CuFe2O4 and CuFe2O4/GO/ZnO ternary nanocomposite revealed that the values of dielectric constant and tangent loss decrease at high frequencies owing to surface charge polarization and intrinsic dipole interactions. The study of the electrical properties of both pure CuFe2O4 and the CuFe2O4/GO/ZnO ternary nanocomposite reveals that the dielectric constant (ε’) and tangent loss (tanδ) exhibit a decreasing trend as the frequency increases. This behavior is attributed to surface charge polarization and intrinsic dipole interactions. At lower frequencies, both samples display elevated values for these properties, which stabilize as the frequency increases beyond 2 MHz. Notably, high AC conductivity is observed in both samples, attributed to increased capacitance and resistance.

A novel heterogeneous biocatalyst based on graphene oxide for synthesis of pyran derivatives

Graphene oxide modified with tryptophan (GO-Trp) has been introduced as a new heterogeneous acid-base biocatalyst for synthesis of some pyran derivatives. GO was prepared according to the Hummer’s method and tryptophan as a low-cost green amino acid is covalently bonded to the surface of GO without any organic or toxic reagents in a green way. The new catalyst was characterized by different spectroscopic methods such as Fourier transform infrared, X-ray diffraction (XRD), etc. …. The results of XRD patterns showed an increase in the distance between the GO plates in the presence of the modifying agent which specifies the presence of amino acid between the GO layers. XPS analysis also confirmed successful modification through the presence of C–N bonds in the structure of the catalyst. In addition, improvements in thermal stability and changes in the morphology of the samples were observed using thermogravimetric analysis and Field emission scanning electron microscopy analysis respectively. Evaluation of the catalyst performance in the synthesis of some benzo[b]pyran and pyrano[3,2-c] chromene derivatives showed presentable results. Seven benzo[b]pyran (4a–4g) and five pyrano[3,2-c] chromene (4h–4l) derivatives were synthesized. GO-Trp as a safe, natural and efficient catalyst, could be reused up to 5 runs for synthesis of pyran derivatives without any significant decrease in its potency. High purity of the products and desirable yields are other points that make the present work more attractive.

Anodic Electrodepositing Bioinspired Cu-BDC-NH2@Graphene Oxide Membrane for Efficient Uranium Extraction.

The challenge of removing trace levels of heavy metal ions, particularly uranium, from wastewater is a critical concern in environmental management. Uranium, a key element in long-term nuclear power generation, often poses significant extraction difficulties in wastewater due to its low concentration, interference from other ions, and the complexity of aquatic ecosystems. This study introduces an anodic electrodeposited hierarchical porous 2D metal-organic framework (MOF) Cu-BDC-NH2@graphene oxide (GO) membrane for effective uranium extraction by mimicking the function of the superb-uranyl-binding protein. This membrane is characterized by its hierarchical pillared-layer structures resulting from the controlled orientation of Cu-BDC-NH2 MOFs within the laminated GO layers during the electrodeposition process. The integration of amino groups from 2D Cu-BDC-NH2 and carboxylate groups from GO enables a high affinity to uranyl ions, achieving an unprecedented uranium adsorption capacity of 1078.4 mg/g and outstanding selectivity. Our findings not only demonstrate a breakthrough in uranium extraction technology but also pave the way for advancements in water purification and sustainable energy development, proposing a practical and efficient strategy for creating orientation-tunable 2D MOFs@GO membranes tailored for high-efficiency uranium extraction.

New insight into interference-free and highly sensitive dopamine electroanalysis

Early diagnosis of Parkinson's disease and hyperprolactinemia based on electrochemical dopamine (DA) sensing appears as an efficient and promising practical diagnostic method. However, the coexistence of DA in real samples with ascorbic acid (AA) and uric acid (UA), which oxidize at potentials close to its own, prevents the accurate electrochemical DA sensing and therefore, hinders the effective diagnosis of these diseases. In this work, we successfully combined the electrostatic proprieties of GO, the electron transfer properties of an AuNPs@MWCNTs nanocomposite and the ability of thiol group of the amino acid l-cysteine to react chemically with carbonyl groups of UA, to develop a novel approach that enabled complete suppression of interference from AA and UA and hence, accurate DA electroanalysis in the conditions close to those of human blood serum. The chemical reaction between l-cysteine and UA was evidenced by monitoring the DPV responses of UA under different conditions. XRD, Raman spectroscopy, XPS and FE-SEM revealed the successful synthesis of GO and AuNPs@MWCNTs. The study of the electrode material (GO-AuNPs@MWCNTs) morphology via FE-SEM and HR-TEM showed that AuNPs@MWCNTs are distributed throughout the exfoliated GO layers. The fabricated sensor was calibrated in the concentration range of 0.5–5 μM, in the presence of the highest blood concentrations of AA and UA for healthy individuals. A linear relationship was observed and the LOD was found to be 1.31 nM (S/N = 3). Furthermore, the sensor showed good electron transfer kinetics, good repeatability and reproducibility, satisfactory long-term stability, and recoveries in human blood serum.

Evaluation of the dispersion properties of graphene oxide/cetyltrimethylammonium bromide for application in nanocomposite materials.

The properties of thermal diffusivity and Z potential of the GONPs/CTAB nanofluid were studied as a function of GO concentration (in the range between 4 and 12% w/v), temperature (35 and 50 °C) and time (30 and 60 min) under ultrasound. In turn, the structural properties of GONPs/CTAB were measured by XRD, Raman, SEM and TEM. The GO previously modified with CTAB was used to obtain a PLA/GO nanocomposite. It was found that the behavior of thermal diffusivity provides information in situ on the dispersion properties of the nanofluid, finding values from 0.0013 to 0.0024 cm2 s-1. The hydrodynamic diameter of the GONP dispersions was also determined to range from 75.83 to 360.3 nm with an increase in Z potential from 17 to 30 mV. The most stable GONPs/CTAB dispersion conditions were 6% w/v GO, 50 °C and 30 min. Under these conditions, the GONPs/CTAB materials present an increase in the spacing between GO layers, associated with a greater multilayer stacking of the GO and CTAB layers. The Raman spectrum allowed us to demonstrate that the modification with CTAB did not affect the crystallinity of GO, which was verified by the intensity ratio of the D band and the G band (ID/IG) for the GO/CTAB samples, with the exception of the GO 6% sample, where an increase in the ID/IG ratio (0.9) was observed compared to GO (0.82), associated with greater intercalation of CTAB between the GO sheets. Finally, an SEM analysis of the PLA/GO nanocomposite was carried out and the homogeneous distribution of GO in PLA was demonstrated when it is used as a filler in proportions of 0.1%. This treatment, in turn, contributed to improving the mechanical flexural properties of the nanocomposite materials.

Environmental policy and the environmental situation in the countries of Central Asia

Sharing the land in today’s day to the unprecedented level of change in the environmental situation are some of the global problems of humanity. Ensure environmental sustainability of the world community in this process, men the opportunity to live in a natural environment to create a comfortable, In the years of independence, important measures regarding the analysis of the environmental situation and environmental policy began to be implemented in the countries of Central Asia . A number of the world’s scientific research and environmental protection are related to various aspects of the environmental situation in the research center. In this research, the shift of the ozone layer, pollution of the oceans of the world, in the loss of the fertile layer of the soil go, be cut out of a tropical forest, desertification, reduction of fresh water sources and biodiversity, the increase of household waste, chemical and neutralization of toxic substances, such as for the study of issues such as the environmental crisis. In this article analyzed ecological policy Central Asian republics in the years of independence.

AuNPs/GO Coated U-Shape Polished SMF Based Localized SPR Sensor for Musta’mal Water Identification

Potential of hybrid gold nanoparticles/graphene oxide (AuNPs/GO) coated single mode fiber (SMF) sensor by exploiting localized surface plasmon resonance (LSPR) effect for Musta’mal water identification was studied. Three structure shapes of fiber optics such as straight-shape, loop-shape and u-shape had been prepared. Three layers of AuNPs with 50 nm in diameter were drop-casted onto the partially unclad polished single mode fiber (SMF) to observe the maximum sensitivity of LSPR. To enhance the LSPR effect, one layer of GO was deposited on top of the AuNPs layer. Two optical light sources with least attenuation (1310 nm and 1550 nm) were employed to study the optical power output as the sensor immersed in different type of water samples. The u-shape SMF portrayed the maximum output power about 24.2 dBm at 1550 nm wavelength. According to the analysis, the deployment of 1550 nm laser wavelength resulted in better sensitivity with 23.2% improvement compared to 1310 nm wavelength. Apparently, the LSPR phenomenon created by AuNPs/GO able to enhance the plasmonic signal up to 51.9% than the uncoated SMF. The thinnest diameter of SMF’s cladding, d=0.1195 mm with U-shape structure exhibited the highest power different of 1.10 dBm, in which suggested the best sensing performance. In conclusion, the optimization of AuNPs/GO u-shape polished SMF resulted in the maximum sensitivity with value of S=72.7 dBm/RIU for Musta'mal water identification.

Printable 2D Materials for Thin Film Batteries and Supercapacitors

Two-dimensional transition metal oxide (TMO) nanosheets are the oxide equivalents of the well-known 2D graphene phase. Compared with graphene, a much wider range of compositions, structures and properties can be realized from TMOs. 2D metal oxides typically have thicknesses of 0.45-2.5 nm, and lateral dimensions between 50 nm and tens of micrometers. Interestingly, although they are oxides, they are very flexible and bendable owing to their thinness. So far, several dozen nanosheet phases have been reported in literature, but many more compositions are possible.Dispersions of TMO nanosheets can be made following one of several solution-phase strategies. Often, they are prepared by chemical delamination of isomorphous layered metal oxide parent phases. In a few cases, the 2D TMO phase can be grown directly bottom-up from an aqueous chemical solution. Either way, the resulting colloidal solutions of 2D single crystal nanosheets can serve in subsequent process step as the basis of a chemical ink suitable for ink jet printing on arbitrary substrates like paper, silicon or flexible polymers. Redox-active nanosheets may also be used as active electrode elements for micro-supercapacitors and flexible thin film batteries.For example, 2D MnO2 nanosheets that are isomorphous to the layered δ-MnO2 (birnessite) phase exhibit high pseudocapacance owing to their beneficial redox properties, relatively high in-plane conductivity and very large specific surface area. Ink-jet printed 2D MnO2 based thin film microsupercapacitors were realized that showed comparable performance with other state of the art systems. However, undoped MnO2 nanosheets exhibit relatively low sheet conductivity. Substitutional doping of 3d metal ions (Co, Fe and Ni) into MnO2 nanosheets improved the volumetric energy density to 1.13 mWh cm−3 at a power density of 0.11 W cm−3. The dopants introduced new electronic states near the Fermi level which enhanced the electronic conductivity within the nanosheets and contributed to the further formation of redox-active 3d surface states. Among these, Fe-doped MnO2 exhibited a significant increase in the carrier density and conductivity, while doping with Ni or Co had a much more limited effect on conductivity. These Fe-doped MnO2 nanosheet-based microsupercapacitors show long cycle life and bendability without performance loss on flexible plastic substrates [1].Following a similar inkjet printing approach, thin film cathodes for Li ion batteries were made using V2O5 nanosheets as charge-storage medium. In this case the conductivity of the electrode was improved by addition of highly conductive 2D MXene (Ti3C2) platelets derived from the parent MAX phase Ti3AlC2. Using LiPF6 in EC/DMC as electrolyte, the hybrid V2O5-MXene electrodes showed a high capacity of 321 mAh g-1 at 1C, 112 mAh g-1 at 10.5C and 92% capacity retention after ~700 cycles [2].As third example, an all inkjet-printed MXene/graphene oxide (GO)/MXene thin film supercapacitor with GO as solid electrolyte phase will be discussed. Here, free water molecules trapped between GO layers enabled proton transport through the electrolyte. The as-made capacitor showed high areal capacitance, good cyclability and power densities comparable with state of the art printed supercapacitors. The specific capacitance could be increased further by addition of liquid electrolyte [3].[1] Y. Wang, Y.-Z. Zhang, Y.-Q. Gao, G. Sheng, J.E. ten Elshof, Nano Energy 68 (2020) 104306.[2] Y. Wang, T. Lubbers, R. Xia, Y.-Z. Zhang, M. Mehrali, M. Huijben, J.E. ten Elshof, J. Electrochem. Soc. 168 (2021) 020507[3] Y. Wang, M. Mehrali, Y.-Z. Zhang, M.A. Timmerman, B.A. Boukamp, P.-Y. Xu, J.E. ten Elshof, Energy Storage Mater. 36 (2021) 318-325.

Surface decoration of polyethylene terephthalate (PET) waste bottle-derived ultrafiltration membrane for enhanced lead ion removal and antifouling properties

PET waste bottle can be potentially used to create eco-friendly ultrafiltration (UF) membranes for water and wastewater treatment. The surface modification and functionalization of PET UF membrane offer opportunities to further heighten the performance of the membrane. In this study, phase inversion technique was used to fabricate PET UF membranes and PET/graphene oxide (GO) nanocomposite membranes through a facile GO suspension coating approach. The GO nanosheets were deposited on the PET UF membrane as a wavy and wrinkly layer. Using lead (Pb) ions and bovine serum albumin (BSA) feed solutions, the filtration performances of the neat PET and GO-PET membranes were evaluated. It was observed that, the Pb ions and BSA removal efficiencies were greatly enhanced by the surface decorated GO. Compared to neat PET, the 0.5GO-PET membrane exhibited improved flux performance by 188% and 61% for the removal of Pb ions and BSA, respectively. A high Pb ion removal of 100% and a BSA rejection of 97% were achieved by 0.5GO-PET membrane. The lower fouling tendency of 0.5GO-PET membrane during long-term filtration was attributed to the increased surface hydrophilicity and smoothness upon the deposition of GO layer. This study demonstrates a sustainable solution for efficient water treatment and heavy metal removal.

Non-Covalent Functionalization of Graphene Oxide with POSS to Improve the Mechanical Properties of Epoxy Composites.

Phenyl polyhedral oligomeric silsesquioxane (POSS) is modified onto the GO surface by using the strong π-π coupling between a large number of benzene rings at the end of the phenyl POSS structure and the graphite structure in the GO sheet, realizing the non-covalent functionalization of GO (POSS-GO). The POSS-GO-reinforced EP (POSS-GO/EP) composite material is prepared using the casting molding process. The surface morphology of GO before and after modification and its peel dispersion in EP are examined. Furthermore, the mechanical properties, cross-sectional morphology, and reinforcement mechanism of POSS-GO/EP are thoroughly examined. The results show that the cage-like skeleton structure of POSS is embedded between the GO layers, increasing the spacing between the GO layers and leading to a steric hindrance effect, which effectively prevents their stacking and aggregation and improves the dispersion performance of GO. In particular, the 0.4 phr POSS-GO/EP sample shows the best mechanical properties. This is because, on the one hand, POSS-GO is uniformly dispersed in the EP matrix, which can more efficiently induce crack deflection and bifurcation and can also cause certain plastic deformations in the EP matrix. On the other hand, the POSS-GO/EP fracture cross-section with a stepped morphology of interlaced "canine teeth" shape is rougher and more uneven, leading to more complex crack propagation paths and greater energy consumption. Moreover, the mechanical meshing effect between the rough POSS-GO surface and the EP matrix is stronger, which is conducive to the transfer of interfacial stress and the strengthening and toughening effects of POSS-GO.

Improved photocatalytic activity of graphene oxide modified Ag-TiO2 for degradation of piroxicam-20 and dehydrogenation of methanol under light irradiation

BackgroundGraphene oxide (GO), an atomic sheet structure made of sp2-bonded carbon atoms with superior optoelectronic, and catalytic properties, has attracted much interest. Incorporating a carbon-rich material, onto metal-loaded TiO2 is reported to increase the photocatalytic properties of resultant composites. MethodsThis research aimed at the deposition of different amounts (1–5 wt.%) of GO using the ultrasonication method on bare TiO2 and Ag (3 wt.%)-TiO2 (AT3) and studied their influence on piroxicam-20 degradation under visible light and methanol dehydrogenation under UV light. The prepared composites' structural, optical, and morphological properties were characterized using XRD, DRS, HR-TEM, FE-SEM, and XPS. Significant findingsHRTEM analysis confirmed the existence of GO layers and spherical-shaped Ag nanoparticles deposited over the TiO2 surface. GO(5 wt.%)@Ag(3 wt.%)-TiO2 (G5@AT3) displayed better photodegradation efficiency (78 %) (k = 0.0082 min−1) under 120 min, and GO(1 wt.%)@Ag(3 wt.%)-TiO2 (G1@AT3) composite produced higher amount (427 mmol) of H2 from photocatalytic dehydrogenation of CH3OH under 5 h relative to TiO2 (2 mmol), AT3 (166 mmol) and GO(5 wt.%)@TiO2 composite (GT5) (11 mmol). HRMS analysis was performed to identify the piroxicam-20 degradation intermediates. Thus, this research provides a proactive strategy highlighting the cooperative effect of Ag and GO loading to improve the photocatalytic efficiency of TiO2 photocatalyst using both UV–visible light irradiation.

Synergistic effects in ZnO nanorod films by pulsed electrodeposition on graphene oxide towards enhanced photocatalytic degradation

In this work the synthesis, characterization and photocatalytic activity of novel graphene oxide-supported ZnO nanostructured film are reported. The ZnO film was deposited onto GO layer in a two-step procedure varying the deposition mode. The electrodeposited ZnO films were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform Infrared (FTIR) spectroscopy and X-ray photoelectron spectroscopy (XPS). The effect of the electrodeposition mode and GO presence on the properties of the ZnO nanostructured film was assessed. The applicability towards the adsorption, photodegradation of methylene blue (MB) for the obtained films was analyzed. The results indicated the electrodeposition pulses result in a strong interaction between ZnO and GO results, lower c-axis strain of the deposited ZnO and higher oxygen vacancies. Synergistic effect of oxygen vacancies and morphology towards degradation performance was indicated. Both adsorption and photocatalysis towards the degradation of MB on the modified ZnO films were observed, 52 % degradation efficiency being recorded in 90 min with a rate constant of 0.00171 min−1 under low UV irradiation, with respect to 5 % corresponding to ZnO film obtained in single step by direct mode and in absence of GO layer. A recycling experiment indicated excellent stability of the photocatalyst, the degradation efficiency reaching 98 % after 3 successive runs.

Hierarchical metal-dielectric-metal nanostructures as SERS sensors for sensitive detection of polycyclic aromatic hydrocarbons

Due to the wide variety, inaccessible self-degradation, high mutagenicity and carcinogenicity of polycyclic aromatic hydrocarbons (PAHs), it still remains challenging to efficiently identify them, especially in real environment. Herein, we develop a bottom-up self-assembly strategy to construct a sandwich-like hierarchical metal-dielectric-metal system composed of mercaptan-modified Au nanospheres-graphene oxide (GO)-Ag nanowires as surface-enhanced Raman spectroscopy (SERS) sensors for sensitive detection of PAHs. The synergistic integration of metallic layers and the organic mercaptan and GO layer not only provides localized enhanced electromagnetic field region which is induced by the nanogap between the top Au nanospheres and the bottom Ag nanowires, but also effectively traps PAHs in the middle layer through hydrophobic interaction of mercaptan and π-π stacking interaction of GO. By rationally optimizing the SERS substrates, the lowest detection concentrations of pyrene, anthracene, phenanthrene and benzo[a]pyrene could be reached, respectively, at 10−8 M, 10−8 M, 10−8 M and 10−7 M. The hierarchical system shows excellent uniformity, reproducibility and is able to identify various types of PAHs in multi-component mixtures as well as in real water environment. This strategy can provide a general platform to identify hazardous pollutants that are hydrophobic or contain benzene rings, such as pesticides, dyes and polychlorinated biphenyls.

A novel approach for recycling agricultural wastes in the synthesis of nanomaterials and their composites

In this study, main focus has been drawn on the utilization of agricultural waste sources to synthesize nanomaterials. Graphene oxide and nanocellulose were prepared using rice husk ash and sugarcane bagasse, respectively. Further, their nanocomposites were also prepared in (1:1) ratio of graphene oxide and nanocellulose. The synthesized nanomaterials from agricultural waste were compared with those prepared from conventional sources through varied characterizations. Scanning electron microscopy, transmission electron microscopy, fourier transform infrared spectroscopy and N2 adsorption-desorption analysis was performed to examine the structural, functional and surface properties of the prepared nanomaterials from different precursors. High resolution imaging revealed better structural characteristics of the nanomaterials fabricated from agri-waste precursors. SEM images showed well exfoliated structure of GO and porous nature of NC. The folded layers of GO represent the presence of hydroxyl groups in the TEM images of GO @ graphite powder. TEM images of nanocellulose showed circular shaped nanoparticles of NC @ cellulose powder. Fourier transform infrared spectroscopy confirmed the presence of all the essential functional groups in the structure of prepared nanomaterials. The nanocomposites prepared using agricultural waste sources and conventional sources were inspected by N2 adsorption-desorption analysis, which demonstrated that the nanocomposites prepared from agri-waste sources exhibits much higher specific surface area than that of prepared from conventional precursors. R2 possess specific surface area of 82.832 m2 g−1 while, R1 possess only 6.721 m2 g−1. N2 adsorption-desorption analysis revealed the pore volume, pore diameter, micropore volume, micropore area and surface area of the prepared nanocomposites. The nanomaterials prepared using agricultural waste products shows desirable characteristics in all aspects which makes them equally applicable in energy storage devices, food packaging, drug delivery systems, nanosensors and water filtration systems.

Sulfonated Pentablock Copolymer with Graphene Oxide for Co2+ Ions Removal: Efficiency, Interaction Mechanisms and Secondary Reaction Products

In this work, sulfonated pentablock copolymer (s-PBC) and s-PBC mixed with graphene oxide (s-PBC_GO) layers were deposited on polypropylene (PP) fibrous filters and tested as active coatings for the removal of cobalt ions from water using adsorption and filtration processes. Some of the coated filters were treated by UV light irradiation to modify their hydrophilic properties. The filters were characterized, before and after the processes, by energy-dispersive X-ray (EDX) analysis and Fourier transform infrared spectroscopy (FT-IR). The Qt (mg/g) values, defined as the weight ratio between the removed ions and the coating layer, were evaluated. In the case of adsorption processes, the best results for the removal of Co2+ ions were achieved by the s-PBC_GO coating, with a Qt of 37 mg/g compared to 21 mg/g obtained by the s-PBC. This was ascribed to the presence of GO, which contains more favorable sites able to adsorb positive ions from the solution. Vice versa, for filtration processes, the s-PBC coated filters show similar or slightly better results than the s-PBC_GO coated ones. Such differences can be ascribed to the shorter contact time between the solution and the coating layer in the case of filtration, with respect to adsorption processes, thus reducing the chance for the ions to be adsorbed on the GO layers before passing through the filter. A collateral effect, observed in this study and enhanced in the case of UV-treated coatings, is the release of radical oxysulfur species. The mechanisms involved in this effect are discussed and identified as a consequence of the interaction between the coating layers and metal ions. In order to identify the mechanism of oxysulfur radicals formation and considering a water sample closer to real water, the Co2+ ions adsorption experiments were conducted in the presence of a competitive organic contaminant (i.e., methyl orange, MO).

The Influences of Pore Blockage by Natural Organic Matter and Pore Dimension Tuning on Pharmaceutical Adsorption onto GO-Fe3O4.

The ubiquitous presence of pharmaceutical pollution in the environment and its adverse impacts on public health and aquatic ecosystems have recently attracted increasing attention. Graphene oxide coated with magnetite (GO-Fe3O4) is effective at removing pharmaceuticals in water by adsorption. However, the myriad compositions in real water are known to adversely impact the adsorption performance. One objective of this study was to investigate the influence of pore blockage by natural organic matter (NOM) with different sizes on pharmaceutical adsorption onto GO-Fe3O4. Meanwhile, the feasibility of pore dimension tuning of GO-Fe3O4 for selective adsorption of pharmaceuticals with different structural characteristics was explored. It was shown in the batch experiments that the adsorbed pharmaceutical concentrations onto GO-Fe3O4 were significantly affected (dropped by 2-86%) by NOM that had size ranges similar to the pore dimensions of GO-Fe3O4, as the impact was enhanced when the adsorption occurred at acidic pHs (e.g., pH 3). Specific surface areas, zeta potentials, pore volumes, and pore-size distributions of GO-Fe3O4 were influenced by the Fe content forming different-sized Fe3O4 between GO layers. Low Fe contents in GO-Fe3O4 increased the formation of nano-sized pores (2.0-12.5 nm) that were efficient in the adsorption of pharmaceuticals with low molecular weights (e.g., 129 kDa) or planar structures via size discrimination or inter-planar π-π interaction, respectively. As excess larger-sized pores (e.g., >50 nm) were formed on the surface of GO-Fe3O4 due to higher Fe contents, pharmaceuticals with larger molecular weights (e.g., 296 kDa) or those removed by electrostatic attraction between the adsorbate and adsorbent dominated on the GO-Fe3O4 surface. Given these observations, the surface characteristics of GO-Fe3O4 were alterable to selectively remove different pharmaceuticals in water by adsorption, and the critical factors determining the adsorption performance were discussed. These findings provide useful views on the feasibility of treating pharmaceutical wastewater, recycling valuable pharmaceuticals, or removing those with risks to public health and ecosystems.