Doped Graphene Oxide Research Articles

Tuning structural and optical properties of GO@Mn-doped Co3O4 hybrid nanocomposite by a facile synthesis

Metal and metal oxide materials are mostly used to tune the optical characteristics. The optical and systemic effects of pure Cobalt Oxide (Co3O4) are examined by knocking out the dissimilar assemblage of Manganese (Mn) ions using the co-precipitation method. Graphene oxide (GO) reduces the optical band gap and enhances the effects of ethical Co3O4 and MnCo3O4 by hydrothermal procedure. The percentage of Mn over pure Co3O4 was 0.09wt.%, 0.18wt.%, 0.27wt.%, and GO doped over MnCo3O4 was 1wt.%. Remarkably, spinel-type cobalt oxide has two participation band gaps at 494nm and 772nm of nanocomposites which then shifted from 494nm to 510nm and 772nm to 779nm with the doping of GO. The result describes that the band gap was minimized from 1.76eV to 1.59eV respectively to accommodate the density of states by doping of Mn ions and GO. Conductivity and optical absorbance were also increased by doping assemblage of Mn ions and GO. XRD peaks show the FCC crystalline structure of Co3O4, and the GO peak disappeared for @MnCo3O4, indicating that GO was completely reduced to rGO during the synthesis process.

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.

Enhanced Electrochemical Performance of NiMn Layered Double Hydroxides/Graphene Oxide Composites Synthesized by One-Step Hydrothermal Method for Supercapacitors.

This study aims to enhance the performance of supercapacitors, focusing particularly on optimizing electrode materials. While pure NiMn layered double hydroxides (LDHs) exhibit excellent electrochemical properties, they have limitations in achieving high specific capacitance. Therefore, this paper successfully synthesized composite materials of NiMn LDHs with varying loadings of graphene oxide (GO) using a hydrothermal method. Systematic physicochemical characterization of the synthesized materials, such as powder X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), field-emission scanning electron microscopy (FE-SEM), and Raman spectroscopy, revealed the influence of GO doping on the microstructure and electrochemical performance of NiMn LDHs. Electrochemical tests demonstrated that the NiMn LDHs/GO electrode material exhibited optimal electrochemical performance with a specific capacitance of 2096 F g-1 at 1 A g-1 current density and 1471 F g-1 at 10 A g-1, when GO doping level was 0.45 wt %. Furthermore, after 1000 cycles of stability testing, the material retained 53.3 % capacitance at 5 A g-1, indicating good cyclic stability. This study not only provides new directions for research on supercapacitor electrode materials but also offers new strategies for developing low-cost and efficient electrode materials.

Batch and column studies for the removal of basic red-46 dye and textile by using magnesium oxide (MgO), strontium titanium trioxide (SrTiO3), cobalt- and iron-doped lanthanum chromium trioxide (Co.Fe.LaCrO3), and cadmium sulfide (CdS)-doped graphene oxide nanocomposites.

Despite efforts to reduce the risk of toxic chemicals, colors, and dyes being released into the environment from urban and industrial areas, there is still cause for concern. Colored water must be filtered and sterilized before it can be used for irrigation. The utilization of metal oxide and nanocomposite materials in wastewater treatment procedures appears to be a viable option for the future. Therefore, different compounds were doped with graphene oxide to identify the best material for dye removal by the adsorption process. According to recent studies, the ideal conditions for graphene oxide-doped magnesium oxide (GO/MgO) are as follows: pH 10 showed the highest adsorption capacity (qe) at 49.4mg/g; an adsorbent dosage of 0.01g/50mL showed 48.3mg/g qe; a shaking time of 30min resulted in 44.2mg/g qe; an initial dye concentration of 100mg/L yielded 53.6mg/g qe; and a temperature of 35°C gave 49.5mg/g qe. For graphene oxide-doped strontium titanate (GO/SrTiO3), the optimum conditions were as follows: pH 10 with 45.8mg/g qe; an adsorbent dose of 0.01g/50mL with 40.5mg/g qe; a shaking time of 30min with 75mg/g qe; and a temperature of 35°C with 44.7mg/g qe. Graphene oxide-doped cobalt and iron-doped lanthanum chromium titanate (GO/Co.Fe.LaCrO3) showed optimum conditions of pH 9 with 34.2mg/g qe; an adsorbent dose of 0.01g/50mL with 27.5mg/g qe; a shaking time of 45min with 33.2mg/g qe; an initial dye concentration of 100mg/L with 37.6mg/g qe; and a temperature of 35°C with 42.5mg/g qe. Graphene oxide-doped cadmium sulfide (GO/CdS) showed the following optimum conditions: pH 8 with 23.1mg/g qe; an adsorbent dose of 0.01g/50mL with 25.5mg/g qe; an initial dye concentration of 75mg/L with 28.3mg/g qe; and a temperature of 35°C with 33.5mg/g qe. The pseudo-first-order model was the best fit only for graphene oxide-doped magnesium oxide (GO/MgO) with an R2 value of 0.966, while the pseudo-second-order adsorption isotherm was the best fit for all four products, with R2 values ranging from 0.991 to 0.998. Additionally, the Langmuir adsorption isotherms provided good results for all four products, with R2 values ranging from 0.957 to 0.985. The Freundlich adsorption kinetics showed satisfactory fit only for graphene oxide-doped magnesium oxide (GO/MgO) and graphene oxide-doped cadmium sulfide (GO/CdS), with R2 values of 0.951 and 0.982, respectively. To examine the characteristics and practicality of the adsorption process, certain thermodynamic variables were calculated. The adsorption capability of the most efficient nanocomposites for the degradation of basic red-46 was significantly affected by various concentrations of heavy metal ions and electrolytes. In dye solutions containing surfactants/detergents, the adsorption efficiency of several effective photocatalysts for basic dyes was significantly reduced. A 0.5M HCl solution was found to be the most effective for desorption. In column investigations, the optimal bed height, flow velocity, and dye intake levels were determined to be 3cm, 1.8mL/min, and 70mg/L, respectively, for maximal adsorption of basic red-46. The adsorption investigation of genuine textile waste products has also been carried out to facilitate the practical deployment of this approach. The methods used in this study were cost-effective, easy to handle, and eco-friendly and involved no hazardous materials in the synthesis, making the resulting materials non-hazardous. All these methods were part of green chemistry.

Enhancing tetrafullerene based photosensors and photovoltaic cells by graphene oxide doping

This study explores the postulated potential of tetrafullerene as a charge transport material when combined with dispersed graphene oxide (GO), over concerns about fullerene’s limited performance in similar devices. Incorporating GO is expected to augment carrier concentration, increase surface area, and reduce operating voltages. Devices fabricated with p-Si/tetrafullerene with varying GO concentration exhibit notable enhancements in both dark and illuminated characteristics. The results demonstrate improved electron concentration and transport, leading to enhanced rectification ratios, ideality factors, and interface state densities across a broad bias and illumination range. Notably, devices doped with 0.2GO exhibit the most promising electrical and photoresponse characteristics, showcasing potential for applications in photosensing and photovoltaics.

Assembled Wood-Polyester Fabric-Hydrogel Janus Evaporator for Sustainable Seawater Desalination.

Solar-driven interfacial evaporation technology is a novel and efficient desalination process that helps alleviate the global shortage of freshwater resources. We developed a Janus evaporator assembled from cotton hydrogel, hydrophilic polyester fabric (PF), and Hydrophobic Wood (PW). By doping graphene oxide and TiO2 as light-absorbing materials within the hydrogel, we achieved a high absorptivity of over 90% across the entire solar spectrum. The hydrophilically modified PF, combined with the PW substrate, provided robust water transport and reduced thermal losses. Subsequent optical path simulations using TracePro74 software verified that the sawtooth light-trapping design of the wood substrate increased multiple light reflections and absorption (compared to a flat structure), enhancing light absorption capabilities. The sawtooth interface also enlarged the evaporation area, further boosting evaporation performance. The cleverly designed evaporator exhibited an evaporation rate of 1.722 kg m-2 h-1 and an efficiency of 83.1% under 1 sun irradiation. Additionally, after applying polydimethylsiloxane to the single surface of the photothermal hydrogel for low surface energy treatment, the resulting Janus structure demonstrated asymmetric wettability that prevented salt ions from accumulating on the irradiated interface. After 8 h of continuous evaporation in saline water (10 wt %), only slight salt crystallization occurred at the edges. The evaporator maintained long-term stability during a 15 day cyclic test, and the produced freshwater fully met the relevant drinking water standards. The components of the evaporator are characterized by simple fabrication, low cost, and eco-friendliness, offering significant application potential in the global context of energy conservation and emission reduction initiatives.

Speckle Pattern Analysis of PVK:rGO Composite Based Memristor Device

AbstractThe memristors are expected to be fundamental devices for neuromorphic systems and switching applications. The device made of a sandwiched layer of poly(N‐ vinylcarbazole) and reduced graphene composite between asymmetric electrodes (ITO/PVK:rGO/Al) exhibits bistable resistive switching behavior. The performance of the memristor can be optimized by controlling the doped graphene oxide. To assess the device performance when it switches between ON and OFF states, optical characterization approaches are highly promising due to their non‐destructive and remote nature. Here, speckle pattern (SP) analysis to this end is introduced. SPs include a huge amount of information about their generating mechanism, which is extracted through statistical elaboration. SPs of the PVK:rGO in different states in situ and examine the conduction mechanism is acquired. The variations in the statistical parameters are attributed to the resistance state of the PVK:rGO with regard to the physical switching mechanism. The resistance/conduction state, in turn, depends on the activity and properties of PVK:rGO memristors, as well as the additional non‐uniformities induced through the variations of density of carriers. The present optical methodology can be potentially served as a bench‐top device for characterization purposes of similar devices during their operating.

Impact of doping on MgB2 superconductors: A comprehensive review

This review introduces fresh insights into the ongoing discussion on doping in the MgB2 superconductor compound, enriching the comparative analysis with previous reviews. Its primary objective is to succinctly summarize and enhance comprehension regarding the influence of doping on the superconducting properties of MgB2. It delves into various aspects, including the impact on the superconducting transition temperature (Tc) and the critical current density (Jc) of the doped samples, while also shedding light on the diverse synthesis methodologies employed by different research laboratories. Throughout the review, the doping agents under scrutiny encompass a wide array, ranging from Li and Be to Bi and Pb. The properties are compared with those undoped samples crafted by the authors of each publication. This review catalogs a range of cited doping agents, including H, Li, Be, C, C15H12O2, diamond, graphene oxide, NaCl, Na2CO3, Mg, Al, Si, K2CO3, CaH2, CaCO3, Sc, Ti, Ni, Cu, Zn, MgGa, GeO2, Se, Rb2CO3, Rh, Pd, Ag, In, Sn, Sb2O3, Te, Cs2CO3, LaB6, La2O3, CeO2, Pr6O11, Nd2O3, Sm2O3, Eu2O3, Gd2O3, Tb2O3, Tb4O7, Dy2O3, Ho2O3, Er2O3, Tm2O3, Yb2O3, Lu2O3, Os, Ir, Pt, Hg, Pb, and Bi. Notably, doping with Be, Na2CO3, C, Al, Rb2CO3, Cs2CO3, Hg and Pb impacts mesh parameters through either Mg or B substitution. Conversely doping with Li, CaH2, Cu, Ag, La2O3, CeO2, Pr6O11, Nd2O3, Gd2O3, Tb4O7, Dy2O3, Ho2O3, Er2O3, Tm2O3, Lu2O3, GeO2, Rh, In, Sb2O3, and Pt exhibits minimal impact on Tc. Moreover, Jc can be substantially enhanced by adding C, Zn, Ag, or Sb2O3. Remarkably, the incorporation of Pd or Pt has shown a substantial increase in Jc with a remarkable improvement of +328 % and +614 % respectively observed at 2 T and 20 K. Doping with rare earth elements such as La2O3, Sm2O3, Eu2O3, Gd2O3, Tb2O3, and Ho2O3 resulted in extraordinary improvement in the value of the critical current density at 20 K under specific conditions, within a range of 0–4 T.

Polyvinylidene fluoride-based loose nanofiltration membrane with graphene oxide intercalation for efficient small organic molecules desalination

Graphene oxide (GO) loose nanofiltration (LNF) membranes show immense potential for the desalination of small organic molecules. However, it remains a significant challenge to compare the performance of GO LNF membranes prepared via different doping methods and study the mechanisms that influence the separation abilities of the membranes. In this study, LNF membranes prepared via three GO doping methods were examined for flux, retention rate, and the separation performance of small organic molecules and inorganic salts. The membranes coated with dopamine (DA) and GO, and subsequently formed polydopamine (PDA)–GO intercalation, showed the best results. A novel LNF membrane material (PVDF/PDA–GO–TFN; PVDF: polyvinylidene fluoride, TFN: thin-film nanocomposite) was developed to enhance the separation performance of small organic molecules and inorganic salts while improving membrane surface stabilization and anti-fouling performance and reducing the “trade-off” effect. The optimal conditions for PDA–GO intercalation and the best combination for interfacial polymerization (IP) were also determined. The intercalation structure was identified via scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy, atomic force microscopy, and Fourier-transform infrared spectroscopy. Furthermore, the separation mechanism of the membrane was determined to be based on the Donnan and steric hindrance effects, according to the correlation analysis of the membrane surface electrical properties (zeta potential), hydrophilicity (contact angle), and pore properties. The PVDF/PDA–GO–TFN LNF membrane displayed a maximum water permeance of 10.45 L/(m2·h·bar), with an 88 % rejection of PEG2000 and a 6.83 % rejection of Na2SO4. Moreover, the membrane exhibited excellent anti-fouling performance and long-term stability, with a mean flux recovery rate of 99.06 % after four cycles of filtration and backwashing tests using small organic molecules and inorganic salt solutions. The inorganic salt retention rate was analyzed using SPSS software, and the results indicated excellent membrane stability. In summary, the preparation of PVDF/PDA–GO–TFN membrane materials provides a novel approach for fabricating LNF membranes that can effectively separate small organic molecules and inorganic salts.

Role of sulfur and phosphorous doping on the electrochemical performance of graphene oxide-based electrodes

Heteroatom doping of graphene oxide (GO) with phosphorous (P), and sulfur (S) was studied. In-situ grown binder-free electrodes of these doped and un-doped GO systems were developed via hydrothermal process. S-GO, P-GO, PS-GO, and un-doped hydrothermally treated GO (H-GO) electrodes were thoroughly investigated through physical and electrochemical characterization. The PS-GO electrode, comprising P (10.90 at%), S (0.3 at%), C (45.54 at%), O (36.36 at%), and Ni (2.38 at%) atoms, exhibited a mixed morphology of a few hundred nanometers doped GO flakes and dissolved Ni foam nanorods. Electrochemical analysis showed, this mixed morphology stimulates the charge storage ability of the PS-GO electrode and achieved a high specific capacity of 1218 C/g, compared to 647 C/g for H-GO at 1 mV/s. Electrochemical analysis revealed, charge was primarily stored through the capacitive charge storage mechanism, where only surface atoms are solely responsible for developing a double layer or facilitating redox reactions between electrode atoms and electrolyte ions. Additionally, the PS-GO electrode demonstrated an energy density of 76.94 Wh/kg at 1 A/g, which is much closer to that of batteries. We anticipate that PS-GO has the potential to be utilized as electrode material in modern energy storage devices.

Investigate the biological activities of Lawsonia inermis extract synthesized from TiO2 doped graphene oxide nanoparticles.

Nanoparticles of titanium dioxide (TiO2) were made by reacting graphene oxide (GO) with Lawsonia inermis leaf extract. X-ray diffraction (XRD) analysis revealed crystalline TiO2 doped GO nanoparticles composed of a variety of anatase phases. Initially, UV-vis spectroscopy was performed to confirm the biogenesis of TiO2 doped GO nanoparticles (NP's). Using SEM, the research showed that the biosynthesized TiO2 nanoparticles were mostly spherical, polydispersed, and of a nanoscale size. Because of the energy dispersive X-ray spectroscopy (EDS) pattern, distinct and robust peaks of titanium (Ti) and oxygen (O) were observed, which were supportive of the formation of TiO2 nanoparticles. By using fourier transform infrared (FTIR) spectroscopy, it was demonstrated that terpenoids, flavonoids, and proteins are involved in the biosynthesis and production of TiO2 doped GO nanoparticles. 2,2-diphenylpicrylhydrazyl (DPPH) assays were conducted to evaluate the free radical scavenging activity of TiO2 doped GO nanoparticles. Additionally, the TiO2 doped GO NPs had enhanced antioxidant activity when compared with the TiO2 matrix. A series of pure TiO2 and TiO2 doped GO nanoparticles (5, 10, 50, and 100 mg/mL) solutions were investigated for their antibacterial activities. In the current study, zebrafish embryos exposed to pure TiO2 and TiO2 doped GO nanoparticles were toxic and suffered a low survival rate based on concentration. During photocatalysis, O2˙ and ˙OH radicals are rapidly produced because of the reactive species trapping experiment. It was estimated that pure TiO2 nanoparticles and those doped with GO were 80% effective in degrading methyl orange(MO) after 120 min, respectively. RESEARCH HIGHLIGHTS: The UV-vis absorption spectra showed a maximum absorbance peak at 290 nm. SEM, the pure TiO2 doped GO NPs exhibit agglomeration and spherical shape. When tested in zebrafish embryos, TiO2 NPs are toxic at high concentrations. GO nanoparticles showed better antioxidant activity. NPs exhibited concentration dependent antioxidative activity.

Microstructure and Biocompatibility of Graphene Oxide/BCZT Composite Ceramics via Fast Hot-Pressed Sintering

Improving fracture toughness, electrical conductivity, and biocompatibility has consistently presented challenges in the development of artificial bone replacement materials. This paper presents a new strategy for creating high-performance, multifunctional composite ceramic materials by doping graphene oxide (GO), which is known to induce osteoblast differentiation and enhance cell adhesion and proliferation into barium calcium zirconate titanate (BCZT) ceramics that already exhibit good mechanical properties, piezoelectric effects, and low cytotoxicity. Using fast hot-pressed sintering under vacuum conditions, (1 − x)(Ba0.85Ca0.15Zr0.1Ti0.9)O3−xGO (0.2 mol% ≤ x ≤ 0.5 mol%) composite piezoelectric ceramics were successfully synthesized. Experimental results revealed that these composite ceramics exhibited high piezoelectric properties (d33 = 18 pC/N, kp = 62%) and microhardness (173.76 HV0.5), meeting the standards for artificial bone substitutes. Furthermore, the incorporation of graphene oxide significantly reduced the water contact angle and enhanced their wettability. Cell viability tests using Cell Counting Kit-8, alkaline phosphatase staining, and DAPI staining demonstrated that the GO/BCZT composite ceramics were non-cytotoxic and effectively promoted cell proliferation and growth, indicating excellent biocompatibility. Consequently, with their superior mechanical properties, piezoelectric performance, and biocompatibility, GO/BCZT composite ceramics show extensive potential for application in bone defect repair.

Enhancement of electro-optical properties of aluminum magnesium oxide thin films through controlled graphene oxide doping

Enhancement of electro-optical properties of aluminum magnesium oxide thin films through controlled graphene oxide doping

Polyaniline/reduced graphene oxide doping induced abundant active sites in enset fiber as an efficient adsorbent material for wastewater treatment

Polyaniline/reduced graphene oxide doping induced abundant active sites in enset fiber as an efficient adsorbent material for wastewater treatment

Zinc oxide doping graphene oxide composites by brush coating for uniformly one-side formation thin films

Zinc oxide doping graphene oxide composites by brush coating for uniformly one-side formation thin films

A physicochemically reformed nanostructured graphene oxide-doped indium magnesium oxide film with enhanced electrical properties

Brush-coated graphene oxide (GO)-doped indium magnesium oxide (InMgO) films were produced in this study. The GO concentration was adjusted to 0, 5, and 15 wt%. The hybrid films were constructed using a one-step facile brush-coating process. The formed hybrid film had an oriented anisotropic morphology with a micro/nanogroove structure due to the shear stress induced by the brush hair movement. This anisotropic structure was used as a liquid crystal (LC) alignment layer. Polarized optical microscopy and pretilt angle analysis revealed the presence of a uniform and homogeneous LC alignment on the hybrid film. The film exhibited excellent light control with the LCs, as well as stable and high optical transmittance in the visible region. The GO doping of InMgO increased its polar anchoring energy and decreased its hysteresis characteristics for LC electronic device applications. These results demonstrate the potential of doping metal oxide films with GO and brush coating them for use in next-generation LC devices.

Room Temperature-Built Gas Sensors from Green Carbon Derivative: A Comparative Study between Pristine SnO2 and GO-SnO2 Nanocomposite

Room temperature-built gas sensors were fabricated from graphene oxide (GO), pristine and doped SnO2 nanostructures. The as-synthesized green carbon derivative (GO) nanomaterials were prepared from waste plastic precursor using Modified Hummer’s methodology. Pristine SnO2 and GO-SnO2 nanocomposite were synthesized employing a wet synthesis technique known as co-precipitation. The as-prepared nanoparticles were investigated for structural crystallographic and morphological features using X-ray diffractometry (XRD) and Transmission electron microscopy (TEM) analytical techniques. High-angle annular dark field (HAADF) and elemental quantifications of the nanopowders were investigated with the Energy dispersive X-ray spectroscopy (EDX). Textural features were determined with the assistance of Brunauer-Emmett-Teller (BET) analyzer. Thermogravimetric analysis (TGA) was performed to ascertain the material stability and degradability of the synthetic materials. Functional group and bond structure analysis was conducted using Fourier-transform infrared (FTIR) spectroscopy. Gas sensor devices were tested for responses towards CH4, H2, LPG, and CO2 gases at 20 ppm concentrations of each. GO-SnO2 nanocomposite sensing device showed optimal detection response towards the respective analyte gases with values of 5.00, 5.08, 4.90 and 3.41 respectively. The prepared nanocomposite showed stability and selectivity towards the target gases in an order of magnitude of H2 > CH4 > LPG > CO2. The optimal gas sensor device’s dynamic gas sensing response was ascribed to the GO doping effect which relatively increased its surface area (46.48 m2g-1) and absorption sites.

The enhancement of intelligent electric response properties in the Polymer Gel Artificial Muscle (PGAM) by incorporating micro/nanoscaled doping and regulation of Graphene Oxide (GO)

To align with the principles of environmental conservation and sustainable progress, a Polymer Gel Artificial Muscle (PGAM) was designed with a sandwich-like configuration, comprising two non-metallic electrode membranes enclosing an electrically-actuated membrane. This PGAM exhibited promising prospects due to its advantageous features such as lightweight, intelligibility, flexibility, and excellent activity. However, despite the widespread utilization of polymer gels, their investigation into intelligent electric response property remained a significant challenge. This study investigated the intelligent electric response properties of the enhanced PGAM by incorporating micro/nanoscaled doping with varying amounts of Graphene Oxide (GO). A control group consisting of a PGAM without GO was also utilized, allowing for the analysis of the regulatory mechanism behind GO-doped PGAM. The findings indicated that a doping amount of 0.03 wt% of GO resulted in a maximum peak difference of 16.08 mN/g in the output force density of PGAM during multiple cycles, with a maximum change rate of 21.13%. The PGAM demonstrated a maximum output force density of 15.06 mN/g during a single cycle when doped with 0.03 wt% of GO. Furthermore, electrochemical analysis of the PGAM revealed that at the same doping amount of 0.03 wt%, the specific capacitance reached its peak value of 324 nF·cm−2, while the resistance reached its minimum value of 1.61 Ω. In summary, the incorporation of GO doping has been found to enhance the intelligent electric response properties of PGAM, thereby offering a novel approach for the advancement of flexible actuators exhibiting superior intelligent electric response property.

Graphene oxide doping in tropical almond (terminalia catappa L.) fruits extract mediated green synthesis of TiO2 nanoparticles for improved DSSC power conversion efficiency

The power conversion efficiency (PCE) of a dye-sensitized solar cell (DSSC) device depends on its semiconductor characteristics. Titanium dioxide (TiO2) nanoparticles are a semiconductor material commonly used in the DSSC device whose characteristics depend on the synthesis process. There are many routes to synthesize TiO2, however, they typically involve hazardous approaches, which may cause risk to the environment. Green synthesis is an environmentally friendly alternative method using ecological solvents that eliminates toxic waste and reduces energy consumption. In this work, tropical almond (Terminalia catappa L.) was used as a natural capping agent in the green synthesis to control the growth of TiO2. In addition, graphene oxide (GO) was used as a dopant to increase the performance of DSSC device. The results are convincing, in which the addition of 0.0017 % GO doping in tropical almond extract mediated green synthesis of TiO2 improved the PCE from 0.85 % to 1.72 %. These results suggest that GO-modified TiO2 nanoparticles green synthesized using tropical almond extract have great potential in the fabrication of DSSC devices with good PCE, low cost, and low environmental impact.

Enhanced proton conductivity of sulfonated poly(ether ether ketone) membranes by constructing cation‐π through doping ammonium ionic liquid and graphene oxide

AbstractIn this paper, sulfonic acid functionalized benzothiazole ionic liquid ([(CH2)3SO3HBth] [H2PO4]) and graphene oxide were combined together through the cation‐π. The sulfonated poly (ether ether ketone) was doped with ionic liquid‐modified GO (IL‐GO) to prepare the SPEEK/IL‐GO composite membrane through the solution casting method. The SO3H and benzothiazole rings act as both proton acceptors and proton donors during proton transport and can replace the role of water in medium‐ and high‐temperature environments, increasing the proton transport sites to a certain extent and increasing the proton conductivity of the SPEEK/IL‐GO composite membrane. The proton conductivity of the SPEEK/IL‐GO‐2 composite membrane achieved an 18.02 mS/cm at 120°C, which is 2.43 times higher than that of the pristine SPEEK membrane. This paper provided a method for increasing proton conductivity and limiting IL loss of the SPEEK membrane.Highlights [(CH2)3SO3HBth][H2PO4] and graphene oxide were combined through cation‐π. The benzothiazole ring and SO3H form acid–base pairs. The proton conductivity of SPEEK/IL‐GO‐2 membrane achieved 18.02 mS/cm.