Solvothermal Technique Research Articles

A comprehensive comparison of plastic derived and commercial Pt/C electrocatalysts in methanol oxidation, hydrogen evolution reaction, oxygen evolution and reduction reaction

This work utilized an innovative and economical remediation method to convert inexpensive waste feedstock into extremely useful catalysts. The procedure centered on polyethylene (PE), an easily accessible substance, and effectively transformed it at a mild temperature utilizing a new solvothermal technique, which entailed the reaction of sulfuric acid with PE chains at 120 °C. Throughout this process, the polymer experienced a pivotal cross-linking stage, resulting in its conversion into carbon materials when exposed to temperatures above 500 °C. To improve the catalytic characteristics, platinum (Pt) was effectively integrated into the resultant carbon matrix using the existing impregnation technique. Further, the catalyst's physicochemical properties were thoroughly analyzed utilizing SEM, FTIR, and XRD techniques. After that, the catalyst's performance was thoroughly evaluated in several electrocatalytic reactions, such as methanol oxidation, oxygen evolution and reduction reactions, and hydrogen evolution. The results of this investigation reveal the impressive electrocatalytic ability of the Pt/C catalyst made from waste plastic. It was found to be comparable to the best commercially available Pt/C catalysts in all the reactions that were examined. This research not only demonstrates the possibility of using waste plastic for catalyst production, but also serves as the first documented example, based on successfully converting waste plastic bags into Pt/C through the conventional Liquid Phase Reduction (LPR) process. This novel method has great potential for sustainable and ecologically responsible catalytic applications.

ZnxFe3-xO4–ZnO heterojunction interfaced with poly(L-DOPA) electron transfer mediator layer for enhanced visible light photocatalytic activity

Z-scheme heterojunctions comprising ZnxFe3-xO4@poly(L-DOPA)@ZnO (ZF@PD@ZnO) were synthesized using solvothermal and precipitation techniques. The study aimed to investigate the impact of the poly(L-DOPA) electron transfer mediator on the photocatalytic performance of ZnxFe3-xO4@ZnO (ZF@ZnO) nanocomposites under visible light irradiation. X-ray diffraction (XRD) and HRTEM analysis confirmed the formation of heterostructures, identifying the crystalline phases of both ZnO and zinc ferrite. BFTEM images revealed a polyhedral shape for all samples, with a tendency toward mild agglomeration. The partial inversion of the zinc ferrite cubic spinel structure was evidenced by FT-IR, XPS, and VSM analyses. Zinc ferrite was found to be ferromagnetic, with cation distributions between tetrahedral (A) and octahedral (B) positions as [Zn0.62+Fe0.43+]A[Fe0.42+Fe1.63+]BO4. The samples exhibited notable photocatalytic activity against Rhodamine B, serving as a model contaminant. Furthermore, the stability and reusability of the samples were examined. Additionally, the study elucidated the photocatalytic mechanism produced by the ternary Z-scheme ZF@PD@ZnO, involving spin-polarized charge carriers. Energy band alignment was evaluated by combining ultraviolet photoelectron spectroscopy (UPS) with UV-Vis spectroscopy. The interplay between band alignment and reactive oxygen species (ROS) generation was discussed in correlation with EPR results. Enhanced ROS generation under visible light illumination, observed in the ZF@PD@ZnO nanocomposite, is mainly due to the addition of the conductive poly(L-DOPA) layer, acting as an electron transfer mediator in the Z-scheme heterojunction, ensuring enhanced charge separation.

Innovative Synthesis of Zeolitic Imidazolate Framework by a Stovetop Kitchen Pressure Cook Pot for Triboelectric Nanogenerator

This study presents a novel approach utilizing solvothermal techniques to synthesize zeolitic imidazolate framework (ZIF‐4) particles. Various properties of the ZIF‐4 particles are investigated to shed light on the structural and morphological characteristics. These ZIF‐4 particles act as a positive triboelectric layer in the fabrication of a triboelectric nanogenerator (TENG) designed for powering electronic devices. The solvothermal‐assisted synthesis ensures the controlled and efficient production of ZIF‐4, optimizing its characteristics for enhanced performance in the TENG. The generated TENG, based on ZIF‐4 particles, determines promising capabilities in converting mechanical energy into electrical power. The highest power of TENG is obtained to be 18 μW at a load resistance of 50 MΩ. This work contributes major insights to the search for sustainable and effective power solutions for electronic gadgets. It emphasizes the potential of ZIF‐4 as a crucial triboelectric material, demonstrating its importance in the advancement of TENGs.

Construction of a nanostructured NiCo2S4/Ni/Ni9S8 composite for energy storage applications

It is necessary to investigate and develop nickel-cobalt sulfide electrodes with superior electrochemical behavior. This work produced the NiCo2S4/Ni/Ni9S8 nanostructure composite (NCS/N/NS) for energy storage in supercapacitors using a solvothermal technique with polyethyleneimine (PEI) as a carbon source, followed by an hour of annealing in an argon atmosphere, and a hydrothermal method with thiourea as a sulfur and nitrogen source. Outstanding electrochemical energy storage properties are provided by NCS/N/NS. The produced electrode material, NCS/N/NS, demonstrated an exceptional capacitance of 1620 F g−1 (696 C g−1) at 1 A g−1 when employed for SCs. An NCS/N/NS was used as the positively charged electrode and the opposite electrode of commercial AC to build an NCS/N/NS//activated carbon (AC) asymmetric device for practical usage. At 1 A g−1, the asymmetric device produced a specific power of 887 W kg−1 and a unique specific energy of 53 Wh kg−1. Moreover, it exhibits a 100% coulombic efficacy and a 95% capacity retention after 3000 cycles, respectively.

Synthesis, characterization and properties of Cr-doped ZnO nanoparticles via a facile solvothermal route

Cr-doped ZnO ([Formula: see text]–0.08) nanoparticles are synthesized using the microwave solvothermal irradiation technique. The final product is calcinated at 450∘C and the nanostructure of the material is investigated using various techniques. In structural studies, XRD analysis shows that the hexagonal wurtzite structure of ZnO is present in the standard JCPDS card. FESEM spectrum reveals the hexagonal shape of the synthesized samples and EDS provides information on the qualitative composition of the nanoparticles. Optical absorbance images show exciton peaks in the UV region, which can be attributed to Cr incorporation into the ZnO lattice, and the optical energy bandgap values are calculated using the tauc plot method. Photoluminescence (PL) emission spectra are measured using PL spectroscopy. Interestingly, vibrating sample magnetometry (VSM) reveals enhancements in the magnetic properties in M–H loops and it is widely used for biological applications like antibacterial activity.

2D/2D Molybdenum Sulfo Selenides/Black Phosphorus Heterostructures for Supercapacitors and Light‐Driven Hydrogen Generation Applications

Abstract2D transition metal dichalcogenide alloys are considered as the promising duo for energy storage and catalyst for light‐driven energy conversion applications due to their novel physicochemical properties. However, heterostructuring with other 2D materials is an effective strategy to enhance the charge storage kinetics as well as comprehensive spectral light response and efficient charge separation. Herein, Molybdenum sulfo selenide (MoSSe)/black phosphorous (BP) heterostructure is synthesized by a one‐pot solvothermal technique, and energy storage and conversion efficiency are characterized. Interestingly, the fabricated symmetric supercapacitor based on the MoSSe/BP hybrid shows an exceptional capacitance of 230 mF cm−2 with an excellent energy density of 31.9 µWh cm−2 and a power density of 805.7 µW cm−2. To validate the experimental findings, Density Functional Theory (DFT) computational simulations are carried out concurrently. The lower diffusion energy barrier for electrolytic ions, in the case of hybrid MoSSe/BP compared to pristine MoSSe, supports the higher charge storage performance. Finally, MoSSe/BP nanocomposites' photocatalytic hydrogen evolution reaction (HER) performance is evaluated under 400 W of UV–vis light, with eosin Y dye acting as a sensitizer and triethanolamine acting as a sacrificial agent. The MoSSe/BP nanocomposite exhibits the maximum photocatalytic HER activity of 5718 µmol h−1 g−1, greater than the bare MoSSe nanostructure.

Synthesis of the oleylamine coated mesoporous Fe3O4 nanospheres and their application towards the efficient chemical fixation of carbon dioxide

The present work reports the successful coating of Fe3O4 nanospheres with oleylamine utilizing a single-step solvothermal technique and its application to carbon dioxide's capture and chemical fixation. The existence of the pure cubic spinel phase of Fe3O4 was established by X-ray diffraction. Fourier transform infrared spectroscopy revealed vibrations corresponding to the oleylamine structure, affirming the coating of oleylamine on Fe3O4 nanospheres. X-ray photoelectron spectroscopy further confirmed the presence of oleylamine on the Fe3O4 surface, along with the constituent elements Fe and O. The nanospheres exhibited a spherical shape with an average diameter of ∼17 nm, shown by morphological investigations. Magnetic properties exhibited a Verwey transition at ∼114 K and a saturation magnetization of ∼60 emu/g. The surface area measurements revealed a pore volume of 0.0717 ccg−1 and surface area of 30.558 m2g-1. The existence of oleylamine on the surface of Fe3O4 nanospheres facilitated the capture of CO2 through chemisorption due to the amine group's high selectivity and the nanospheres' large surface area. In the presence of styrene oxide and tetra-n-hexyl ammonium bromide (THAB), the oleylamine-coated Fe3O4 nanospheres successfully converted CO2 to styrene carbonate. The magnetic core and high thermal stability of the material make it suitable for recyclability for the fixation of CO2 into products with added value. This work presents a promising approach for CO2 capture and utilization using Fe3O4 nanospheres coated with oleylamine, with potential applications in carbon capture and utilization technologies.

Thermal-based Zinc-Oxide-Coated Smart Fabric for Thermochromic Applications

The present study focuses on developing a thermochromic device with a flexible substrate through the coating of cotton fabric with ZnO (Zinc oxide) by solvothermal synthesis technique. Here, ZnO is used as the thermochromic layer for the fabrication work, and it is suitable for textile and wearable applications as it is non-toxic to human skin. This device is designed and fabricated in order to gain better insight into the role of ZnO in thermochromic applications. Here, 3D nanostructures of ZnO are grown on the surface of cotton fabric using a simple and cost-effective solvothermal synthesis approach. The coated fabrics are investigated to determine their structure, morphology, composition, electrical, optical and emissivity properties using an X-ray diffraction (XRD), field-emission scanning electron microscope (FE-SEM), current-voltage (I-V) characteristics, ultraviolet protection factor (UPF) etc. From the morphology study, uniformly packed ZnO nanorods with growth in the c-axis direction are observed. The ZnO nanostructures are known to have excellent UPF when exposed to solar radiation and showed UPF value of 112.48. It is found that coated fabrics have increased electrical conductivity under optical excitations and also enhanced the reflectance. Moreover, based on the emissivity analysis coated ZnO cotton fabric showed the emissivity of 0.95, which is higher and has greater radiation protection than that of bare cotton fabric. Hence, the developed thermochromic device has potential for use in the future in textile and wearable based thermochromic application.

Vinorelbine-loaded multifunctional magnetic nanoparticles as anticancer drug delivery systems: synthesis, characterization, and in vitro release study.

In this study, a multifunctional therapeutic agent combining chemotherapy and photothermal therapy on a single platform has been developed in the form of vinorelbine-loaded polydopamine-coated iron oxide nanoparticles. Vinorelbine (VNB) is loaded on the surface of iron oxide nanoparticles produced by a solvothermal technique after coating with polydopamine (PDA) with varying weight ratios as a result of dopamine polymerisation and covalent bonding of thiol-polyethylene glycol (SH-PEG). The VNB/PDA/Fe3O4 nanoparticles have a saturation magnetisation value of 60.40 emu/g in vibrating sample magnetometry, which proves their magnetisation. Vinorelbine, which is used as an effective cancer therapy agent, is included in the nanocomposite structure, and in vitro drug release studies under different pH conditions (pH 5.5 and 7.4) and photothermal activity at 808 nm NIR laser irradiation are investigated. The comprehensive integration of precise multifunctional nanoparticles design, magnetic response, and controlled drug release with photothermal effect brings a different perspective to advanced cancer treatment research.

Preparation of surface molecular imprinting fluorescent sensor based on magnetic porous silica for sensitive and selective determination of catechol.

A magnetic fluorescent molecularly imprinted sensor was successfully prepared and implemented to determine catechol (CT). Fe3O4 nanoparticles were synthesized by the solvothermal technique and mesoporous Fe3O4@SiO2@mSiO2 imprinted carriers were prepared by coating nonporous and mesoporous SiO2 shells on the surface of the Fe3O4 subsequently. The magnetic surface molecularly imprinted fluorescent sensor was created after the magnetic mesoporous carriers were modified with γ-methacryloxyl propyl trimethoxy silane to introduce double bonds on thesurface of the carries and the polymerization was carried out in the presence of CT and fluorescent monomers. The magnetic mesoporous carriers were modified with γ-methacryloxyl propyl trimethoxy silane and double bonds were introduced on the surface of the carriers. After CT binding with the molecularly imprinted polymers (MIPs), the fluorescent intensity of the molecularly imprinted polymers (Ex = 400nm, Em = 523nm) increased significantly. The fluorescent intensity ratio (F/F0) of the sensor demonstrated a favorable linear correlation with the concentration of CT between 5 and 50μM with a detection limit of 0.025μM. Furthermore, the sensor was successfully applied to determine CT in actual samples with recoveries of 96.4-105% and relative standard deviations were lower than 3.5%. The results indicated that the research of our present work provided an efficient approach for swiftly and accurately determining organic pollutant in water.

Novel mixed heterovalent (Mo/Co)Ox-zerovalent Cu system as bi-functional electrocatalyst for overall water splitting

A novel hybrid ternary metallic electrocatalyst of amorphous Mo/Co oxides and crystallized Cu metal was deposited over Ni foam using a one-pot, simple, and scalable solvothermal technique. The chemical structure of the prepared ternary electrocatalyst was systematically characterized and confirmed via XRD, FTIR, EDS, and XPS analysis techniques. FESEM images of (Mo/Co)Ox–Cu@NF display the formation of 3D hierarchical structure with a particle size range of 3–5 µm. The developed (Mo/Co)Ox–Cu@NF ternary electrocatalyst exhibits the maximum activity with 188 mV and 410 mV overpotentials at 50 mA cm−2 for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), respectively. Electrochemical impedance spectroscopy (EIS) results for the (Mo/Co)Ox–Cu@NF sample demonstrate the minimum charge transfer resistance (Rct) and maximum constant phase element (CPE) values. A two-electrode cell based on the ternary electrocatalyst just needs a voltage of about 1.86 V at 50 mA cm−2 for overall water splitting (OWS). The electrocatalyst shows satisfactory durability during the OWS for 24 h at 10 mA cm−2 with an increase of only 33 mV in the cell potential.

Electrochemical energy storage application of MOF-derived porous NiO thin films synthesized by solvothermal route

Metal oxides are the most suitable materials for supercapacitors because of their strong electrical characteristics and cheap prices. Owing to its large surface area, controlled pore structure, uniformity, the metal-organic frameworks are employed as inventive material for electrodes in the field of energy storage. In this report, Ni-MOFs have been prepared on conducting stainless steel substrates using a solvothermal technique with different Ni concentrations. Further, these films were annealed at 350 °C for getting NiO phase. The crystalline nature of MOF-derived NiO is confirmed by XRD. The surface morphology of the films has been studied with FE-SEM, showing a nanosheet-like structure. Consequently, electrochemical tests on NiO electrodes were performed in 1 M KOH with a potential window of -0.2–0.5 V. The NiO electrode deposited with 0.3 M concentration delivers a specific capacity of 680 C g−1 at a current density of 0.5 mA cm−2, an energy density of 22.40 Wh kg−1 at a power density of 2.4 kW kg−1 and good cyclic performance with 96% retention after 5000 cycles. The synthesized MOF derived NiO showed excellent specific capacity and good cycle stability due to their large surface area, porous and more durable structure. Hence, the synthesis approach designated here may provide an efficient way to develop MOF-derived NiO for effective supercapacitor applications.

Synergistic integration of Ni-metal organic framework/SnS2 nanocomposite and nickel foam electrode for ultrasensitive and selective electrochemical detection of albumin in simulated human blood serum

Albumin is a vital blood protein responsible for transporting metabolites and drugs throughout the body and serves as a potential biomarker for various medical conditions, including inflammatory, cardiovascular, and renal issues. This report details the fabrication of Ni-metal organic framework/SnS2 nanocomposite modified nickel foam electrochemical sensor for highly sensitive and selective non enzymatic detection of albumin in simulated human blood serum samples. Ni-metal organic framework/SnS2 nanocomposite was synthesized using solvothermal technique by combining Ni-metal–organic framework (MOF) with conductive SnS2 leading to the formation of a highly porous material with reduced toxicity and excellent electrical conductivity. Detailed surface morphology and chemical bonding of the Ni-MOF/SnS2 nanocomposite was studied using scanning electron microscopy, transmission electron microscopy, Fourier transform infra-red, and Raman analysis. The Ni-MOF/SnS2 nanocomposite coated on Ni foam electrode demonstrated outstanding electrochemical performance, with a low limit of detection (0.44 μM) and high sensitivity (1.3 μA/pM/cm2) throughout a broad linear range (100 pM–10 mM). The remarkable sensor performance is achieved through the synthesis of a Ni-MOF/SnS2 nanocomposite, enhancing electrocatalytic activity for efficient albumin redox reactions. The enhanced performance can be attributed due to the structural porosity of nickel foam and Ni-metal organic framework, which favours increased surface area for albumin interaction. The presence of SnS2 shows stability in acidic and neutral solutions due to high surface to volume ratio which in turn improves sensitivity of the sensing material. The sensor exhibited commendable selectivity, maintaining its performance even when exposed to potential interfering substances like glucose, ascorbic acid, K+, Na+, uric acid, and urea. The sensor effectively demonstrates its accuracy in detecting albumin in real samples, showcasing substantial recovery percentages of 105.1%, 110.28%, and 91.16%.

Structural, morphological and optical properties of ZnFe2O4-decorated reduced graphene oxide nanocomposite for antibacterial applications

In this study, the zinc ferrite decorated reduced graphene oxide (ZnFe2O4-rGO) was synthesised by using a simplified one-pot solvothermal technique. The synthesised nanomaterials were examined for structural, morphological and optical characteristics is greatly aided by the XRD, HRTEM, SAED, EDX spectroscopy, Raman spectroscopy and UV–Vis spectroscopy. The crystallite size calculated from XRD and HRTEM of the ZnFe2O4-rGO nanocomposite was around 10 nm. The presence of desired elements in the synthesised nanomaterials was confirmed using EDX spectroscopy. The Raman spectroscopy aided in identifying the active functional modes. The absorption maximum (λmax) was found to be approximately ∼310 nm and the optical bandgap of ZF was reduced from 2.1 eV to 1.97 eV in ZF-rG. The antibacterial activity of ZnFe2O4-rGO nanocomposite was discussed against Enterococcus faecalis, Staphylococcus aureus, Klebsiella pneumonia and Escherichia coli bacteria at different concentrations by agar gel diffusion method among which the highest bacterial growth inhibition was seen in Klebsiella pneumonia in all different concentrations in which 86% at 100 μg/ml was the most effective.

Optimized Charge Dynamics of Sr2Fe2O5/rGO Composite Electrodes: Redefining Supercapacitor Efficiency

Mixed transition metal oxides have become highly effective electrode materials due to their remarkable cyclic stability and improved capacitance, which has consequently led them to display exceptional electrochemical performance. In this work, a facile synthesis of Sr2Fe2O5/reduced graphene oxide composites was carried out through a solvothermal technique to investigate the electrochemical performance. X-ray diffraction patterns confirmed the cubic perovskite structure of Sr2Fe2O5. The morphological analysis revealed well-defined grains with sharp boundaries, having uniformly distributed porous regions. The stoichiometric ratios of sample compositions were confirmed using elemental analysis. The electrolyte employed for the electrochemical characterizations was 1 M potassium hydroxide (KOH), carried out using three-electrode cell. The composite sample Sr2Fe2O5/15% reduced graphene oxide showed excellent electrochemical performance compared to other samples. It demonstrated a maximum specific capacitance of ∼360.29 F g−1 at a lower scan rate of 0.01 V s−1, as observed using cyclic voltammetry. The electrochemical analysis of this electrode through the GCD system has a high value of capacitance ∼1110 F g−1 followed by a high energy density value of ∼32.76 Wh kg−1, respectively. The Nyquist plot revealed less barrier to charge transfer. Therefore, the comprehensive investigation of this electrode material suggested that this as-synthesized composite could be utilized in high-performance energy storage devices.

Surface Modification of Bi2Te3 Nanoplates Deposited with Tin, Palladium, and Tin/Palladium Using Electroless Deposition

Surface-modified nanoplate-shaped thermoelectric materials can achieve good thermoelectric performance. Herein, single-crystalline Bi2Te3 nanoplates with regular hexagonal shapes were prepared via solvothermal techniques. Surface modification was performed to deposit different metals onto the nanoplates using electroless deposition. Nanoparticle-shaped tin (Sn) and layer-shaped palladium (Pd) formed on the Bi2Te3 nanoplates via electroless deposition. For the sequential deposition of Sn and Pd, the surface morphology was mostly the same as that of the Sn-Bi2Te3 nanoplates. To assess the thermoelectric properties of the nanoplates as closely as possible, they were compressed into thin bulk shapes at 300 K. The Sn-Bi2Te3 and Sn/Pd-Bi2Te3 nanoplates exhibited the lowest lattice thermal conductivity of 1.1 W/(m·K), indicating that nanoparticle-shaped Sn facilitated the scattering of phonons. By contrast, the Pd-Bi2Te3 nanoplates exhibited the highest electrical conductivity. Thus, the highest power factor (15 μW/(m∙K2)) and dimensionless ZT (32 × 10−3) were obtained for the Pd-Bi2Te3 nanoplates. These thermoelectric properties were not as high as those of the sintered Bi2Te3 samples; however, this study revealed the effect of different metal depositions on Bi2Te3 nanoplates for improving thermoelectric performance. These findings offer venues for improving thermoelectric performance by sintering nanoplates deposited with appropriate metals.

V2O5 coral microspheres: High performance electrode material for Li-ion supercapacitor

Energy storage devices forms lifeline for most modern devices. The short life cycle and lower power density of batteries has prompted development of supercapacitors as potential alternatives. Li-ion supercapacitors, is an emerging class of energy storage devices. Natural abundance and availability of variable oxidation states make V2O5 an attractive electrode material. Here, we report synthesis of coral microspheres of V2O5 using low temperature solvothermal technique, as electrode material for Li-ion supercapacitor. The annealing temperature plays a cucial role in formation of microspherical aggregates, dictates their surface area and hence the energy storage performance. Samples annealed at 400 °C showed specific capacitance of ∼360 F/g at current density of 0.5 A/g. Our studies suggest that V2O5 based nanostructures holds significant potential for development of hybrid Li-ion supercapacitors.

Rambutan-like Ni0.5Zn0.5Fe2O4 nanospheres with tunable N-doped carbon shell as anode materials for high performance lithium-ion batteries

Multi-metal oxides have abroad application prospects as anode materials in lithium-ion batteries (LIBs) due to their adjustable chemical composition and plentiful active sites. In this study, rambutan-like Ni0.5Zn0.5Fe2O4 nanosphere are prepared by incorporating Zn into NiFe2O4, using a self-templating solvothermal technique. Then, Ni0.5Zn0.5Fe2O4@ N-doped carbon (NC) shell materials with different thickness of NC shell are obtained via coating different amount of dopamine followed by carbonization. As a LIBs anode material, the effects of NC shell thickness on electrochemical properties are discussed, and the Ni0.5Zn0.5Fe2O4@NC with 15 nm NC shell delivers 953.6 mA h g−1 specific capacity after 400 cycles at a current density of 1 A g−1, while the reversible capacity reaches 1124.3 mA h g−1 at the current of 0.1 A g−1. These results confirm that the appropriate NC shell thickness can effectively buffer the volume change and improve the electronic conductivity, accordingly improve the capacity and cycle stability of the electrode material. Furthermore, LiCoO2//Ni0.5Zn0.5Fe2O4@NC lithium-ion full cells are successfully assembled, and the electrochemical evaluation results demonstrate that they exhibit excellent lithium storage performance and promising application prospect.

Ultrasensitive detection of ornidazole–antibiotic drug residues in water using NiMOFs functionalized MWCNT modified electrode

Nitroimidazole-based drugs are widely used as an antibiotic for the treatment of anaerobic bacterial and parasite illnesses. The widespread use of these drugs in animal feed and the consequent environmental pollution have become significant concerns in recent years. Simple, sensitive, and rapid detection of the antibody in various real samples is demanding research interest. Herein, we report a Nickel-metal organic framework functionalized Multiwalled Carbon nanotubes modified glassy carbon electrode (MWCNT@NiMOFs) as an ultrasensitive and rapid voltammetric sensor for the detection of ornidazole (ORDZ) in a neutral pH solution. The MWCNT@NiMOFs were prepared using a microwave-assisted solvothermal technique accompanied by an ultrasonication method. The designed MWCNT@NiMOFs offered a low charge transfer resistance (Rct) of 141 Ω along with excellent electrocatalytic activity, and high current density at the lowered cathodic peak potential (-0.62 V vs Ag/AgCl) for ORDZ detection. The surface adsorption capacity (Γs) in terms of surface excess and heterogeneous charge transfer rate constant (k0) of the MWCNT@NiMOFs were calculated to be 3.29 × 10-9 mol cm−2 and 5.33 × 10-3 cm s−1, respectively. Under an optimal working condition, differential pulse voltammetry measurements of ORDZ have shown concentration linearity in a window, 100 nm to 10 µM range with excellent sensitivity, 5.69 × 10-5A µM−1 cm−2, and detection limit, 26 nM (3.3/s). The designed MWCNT@NiMOFs offered appreciable reproducibility, and repeatability up to 30 days of storage time. The real-time quantitative evaluation of ORDZ in human urine and tap water specimens was done along with ∼ 100 % recovery values. Since the new approach is simple, selective, and separation-free, it can be extendable to a variety of real-time practical applications.

Preparation of surface-active carbon dots with fluorocarbon and hydrocarbon hybrid chains via a one-pot solvothermal technique and their characterization and potential applications

Amphiphilic carbon dots (CDs) are new surface-active materials that exhibit several advantages over conventional small surfactants, such as improved stability and reduced toxicity. However, unlike for conventional small surfactants, amphiphilic CDs that simultaneously exhibit excellent surface and interfacial activities have never been achieved. Herein we prepare new amphiphilic CDs with fluorocarbon and hydrocarbon hybrid hydrophobic chains (FH-CDs) using a facile one-pot solvothermal technique. The obtained FH-CDs showed excellent surface and interfacial activities, and reduced the surface tension at critical micelle concentration and the oil-water interfacial tension to 16.7 and 2.2 mN/m, respectively. Comparison with control CDs bearing only non-hybrid hydrophobic chains demonstrated that decorating CDs with fluorocarbon and hydrocarbon hybrid chains contributed to the excellent interfacial activity, while only fluorocarbon chains contributed to good surface activity. The excellent surface and interfacial activities made FH-CDs good emulsifiers for the formation of stable water-in-oil emulsions and for the preparation of relatively uniform polystyrene spheres via emulsion polymerization. Moreover, FH-CD was a good wetting agent, whose aqueous solution could wet numerous different surfaces, including the commonly non-wettable amphiphobic polytetrafluoroethylene.