Catechol Research Articles

PH-Responsive Carrier-Free Polyphenol Nanoparticles Assembled by Oxidative Polymerization with Enhanced Stability and Antioxidant Activity for Improved Bioaccessibility.

Encapsulation of plant polyphenols with micro-/nano-carriers for enhanced bioavailability has been well documented, but the preparation of these carriers and subsequent loading of polyphenols is a multiple process, which is generally complicated with potentially unexpected negative effects on the bioactivity of the polyphenols. Here, we reported a convenient method to assemble carrier-free polyphenol nanoparticles (NPs) based on oxidative coupling polymerization. The effectiveness was assessed with five different polyphenols including pyrocatechol (PY), catechin (CA), epigallocatechin gallate (EGCG), tannic acid (TA), and proanthocyanidin (PC). The structural characteristics of these assembled nanoparticles (PY NPs, CA NPs, EG NPs, TA NPs, and PC NPs) were systematically analyzed with dynamic light scattering (DLS), transmission electron microscopy (TEM), UV-visible spectroscopy, and Fourier transform infrared spectroscopy (FTIR). All NPs were colloidally stable with varying NaCl concentrations from 0 to 300 mM, were acid-resistant and alkali-intolerant, and were suitable for oral administration. An array of antioxidant assays further confirmed the superior antioxidant capabilities of NPs over Trolox and polyphenol monomers, indicating that the oxidative polymerization of polyphenols did not compromise the polyphenol activity of NPs. The in vitro simulated digestion studies validated that these responsive NPs were actually gastrointestinal pH-responsive and applicable to the gastrointestinal physiological environment. The bioaccessibility assessments by using a static in vitro digestion model revealed that better results were achieved with NPs than polyphenol monomers, with TA NPs showing about 1.5-fold higher bioaccessibility than other polyphenol nanoparticles. The present study with five polyphenols demonstrated that the oxidative polymerization of polyphenols provides an effective platform to assemble various carrier-free NPs with enhanced antioxidant activity, favorable stability, and improved bioaccessibility, which could be used promisingly as a functional food ingredient in food matrices or as oral drug delivery candidates for helping to manage human health or treating various gastrointestinal disorders in both the pharmaceutical and nutritional fields.

Investigation of the adsorption and sensor properties of resorcinol (RSL) on X9N9 (X = Al, B, Ga, In) nanorings by DFT and QTAIM analysis with solvent effects

De-aromative oxygenation of resorcinol is recognized as an important process that produces a variety of bioactive chemicals. Hence, we evaluated the sensing application by utilizing density functional theory to study the resorcinol (RSL)-X9N9 (X = Al, B, Ga, and In) nanoring interaction. We saw that RSL had a strong interaction with every ring. A charge transfer occurs between nanorings and RSL, causing dipole moment to be induced. The band gap energies of all complexes are less than that of RSL. In vacuum the band gap energies of the complexes are less than that of pristine rings while in water, RSL-Ga/In-N complexes, the band gap energies are higher than that of pristine rings. In vacuum all the complexes, except B9N9-RSL have higher adsorption energies. In water phase, Al9N9/Ga9N9-RSL complexes have higher adsorption energies. These values suggest they are good dopants for RSL. The electrical conductivity and work function are significantly altered as a result of the alteration in the Frontier Molecular Orbitals (FMOs) energies of the nanorings following interaction. It is possible to use the X9N9 nanorings for RSL as both an electronic sensor and a work function-based sensor. The extended recovery time of RSL with X9N9, however, indicates that it can be used to store RSL or remove it from a specific environment. Atom in Molecules (AIM) analysis predicts the comprehension reactivity, chemical bonding, and the creation of compounds. The present work can be extended to investigate the effect of coinage metal doping with nanorings to study doping effects and drug delivery carrier properties.

Identification of the toxin components of Rhizoctonia solani AG1-IA and its destructive effect on plant cell membrane structure.

Rice sheath blight is a fungal disease caused mainly by Rhizoctonia solani AG1-IA. Toxins are a major pathogenic factor of R. solani, and some studies have reported their toxin components; however, there is no unified conclusion. In this study, we reported the toxin components and their targets that play a role in R. solani AG1-IA. First, toxins produced by R. solani AG1-IA were examined. Several important phytotoxins, including benzoic acid (BZA), 5-hydroxymethyl-2-furanic aid (HFA), and catechol (CAT), were identified by comparative analysis of secondary metabolites from AG1-IA, AG1-IB, and healthy rice. Follow-up studies have shown that the toxin components of this fungus can rapidly disintegrate the biofilm structure while maintaining the content of host plant membrane components, thereby affecting the organelles, which may also explain the lack of varieties highly resistant to sheath blight.

The Molecular Structural Analysis of Biologically Important Catechol Molecule: An Integrative Perspective from Experiments and Futuristic Tools

Background: Catechol is a phenolic molecule found naturally in plants. It is also known as pyrogallic acid or 1, 2-dihydroxybenzene. Catechol is currently produced commercially by decarboxylating gallic acid at high temperatures and pressures. Aims and Objectives: This research aimed to understand the biological importance of catechol and perform molecular structural analysis on catechol molecules. Methods: Catechol (1, 2, dihydroxy benzene) was studied via computational analysis by employing the use of DFT and B3LYP methods. Hirshfeld analysis was carried out to investigate crystal intermolecular interactions, and the NBO study was performed to study chemical donating and accepting interactions. Moreover, the computational study was performed using FTIR, HNMR and other instrumentation like AIM theory for circular dichroism data. Results: Furthermore, the surface iso-projection study and binding energy results did prove to run in alignment with experimentally obtained values from the computational studies. Fukui functional study and molecular electrostatic potential were utilized in the study to investigate interactions between anionic and cationic sites of catechol. In addition, molecular dynamic simulations revealed that biomolecular stability was also present. Thus, the antibiotic efficacy of catechol displayed chemical oxidative interactions that exhibited close chemical correlations with ascorbic acid, ellagic acid, and gallic acid. Conclusion: The catechol has been examined experimentally and theoretically. The results were compared with catechol spectra, including IR and UV-visible spectra generated through computer analysis. The experimentally observed spectra were found to be in parallel with theoretical data. According to drug-likeness investigations, the following compounds, gallic acid, ellagic acid, and ascorbic acid, were found to be closely related to catechol as an antibiotic. Hence, it can be concluded that catechol, whether in its entirety or in a portion, is a potent antibacterial, anti-inflammatory, and anti-malarial drug.

Porphyrin-based covalent organic framework integrated with nitrogen doped carbon nanotube as electrode modifier for selective and simultaneous detection of hydroquinone and catechol with high sensitivity

A novel Co-porphyrin-based covalent organic framework (TT-COF(Co)) was synthesized and further integrated with nitrogen doped carbon nanotube (N-CNTs), which was used as electrode modifier material for the application in selective and simultaneous electrochemical detection of hydroquinone (HQ) and catechol (CA). The successful formation of TT-COF(Co)/N-CNTs nanocomposite was confirmed through a series of different characterization techniques, including scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray diffraction (XRD), fourier-transform infrared spectroscopy (FT-IR), and X-ray photoelectron spectroscopy (XPS). Electrochemical results indicated that TT-COF(Co)/N-CNTs nanocomposite modified electrode had excellent sensing performance for HQ and CA in phosphate buffer, enabling selectively and simultaneously determination of these two dihydroxybenzene isomers. Under optimal testing conditions, linear calibration curves for the selective determination of HQ or CA in the presence of 30 µM of the corresponding isomers were obtained over the concentration range of 0.01–500 µM. The linear ranges for the simultaneous determination of HQ and CA were 0.003–300 µM, with detection limits of 0.81 nM for HQ and 0.74 nM for CA, respectively. The sensor also demonstrated satisfactory selectivity and stability, and was successfully used to analyse HQ and CA in real water samples. Our work made a useful contribution to strategical design of functionalized COFs materials for electrochemical sensing applications.

Ultrasensitive simultaneous determination of hydroquinone and catechol by Ni3ZnC0.7/Ni porous composites derived from Ni/Zn-MOF

Rational constructing metal–organic frameworks (MOFs) based composite materials with outstanding catalytic capability is vital to accomplish high-performance electrochemical sensors. In this paper, the precursor Ni/Zn-MOF was fabricated by a simple one-step solvothermal method, and then the Ni nanoparticle-supported porous microsphere composites (Ni3ZnC0.7/Ni) were obtained by pyrolysis in N2 atmosphere. The physicochemical characteristics of the as-prepared Ni3ZnC0.7/Ni were studied by XRD, SEM, EDS, TEM, FTIR and XPS, and their electrocatalytic activity were tested by Cyclic voltammetry (CV) and differential pulse voltammetry (DPV). On this basis, an electrochemical sensor strategy for the simultaneous determination of hydroquinone (HQ) and catechol (CC) with Ni3ZnC0.7/Ni modified glassy carbon electrode (GCE) was proposed. In addition, they were applied to the electrochemical simultaneous detection of HQ and CC for the first time. Compared with NiC and ZnC modified electrode, the Ni3ZnC0.7/Ni composites modified electrode can significantly enhance electrocatalytic activity and improve the selectivity and sensitivity of the detection of HQ and CC. The performance was due to increasing the active surface area of the modified electrode and the Ni atom has excellent electrocatalytic capability to dihydroxybenzene. The experimental results exhibits that the composite was used to achieve simultaneous detection of HQ and CC in single-component or two-component solutions with satisfactory result. It has a low limit of detections (LOD = 3σ/k) (HQ: 0.14 μM, CC: 0.21 μM) and a wide detection range (HQ: 0.3–100.0 μM, CC: 0.5–100.0 μM). Meanwhile, the constructed sensor has been successfully employed for determination of HQ and CC in Yellow River water and tap water, and obtains good recovery rate. This work develops a new approach for design and engineering of MOF materials for electrochemical sensors and environmental monitoring.

Development of a sensitive and selective catechol amperometric sensor based on a novel In2O3-doped CuO decorated mesoporous carbon nanocomposite

Catechol is known for its reactivity with various biomolecules, posing potential health risks. Therefore, in this research, we have successfully developed an electrochemical sensor with high sensitivity and selectivity for detecting catechol (CC). The sensor utilizes a novel In2O3-doped CuO decorated Mesoporous Carbon Nanocomposite (In2O3.CuO@MC) as the sensing material, which is applied to fabricate a glassy carbon electrode (GCE). The suitability of the In2O3.CuO@MC nanocomposite as a sensing material was thoroughly examined using various characterization techniques. The developed sensor exhibited remarkable performance, enabling the accurate catechol determination across a wide concentration range, from 0.5 to 3031 µM, in a neutral phosphate buffer solution. This sensor demonstrated a high sensitivity of 0.3803 µAµM−1cm−2 and an impressive detection limit of 0.048 µM. The sensor's exceptional sensitivity and selectivity make it capable of precisely quantifying catechol from real samples. Its robustness is further highlighted by its excellent reproducibility, repeatability, and stability. As a result, this sensor proves to be a reliable and effective tool for precise catechol determination.

MnO@C composites derived from MOFs coated with reduced graphene oxide for simultaneous detection of catechol and hydroquinone

AbstractIn this work, manganese‐based metal‐organic frameworks (MnBDC) were synthesized by solvothermal method and physically mixed with pre‐prepared graphene oxide (GO) to obtain GO/MnBDC, which were calcined to give MnO@C composite coated with reduced graphene oxide (rGO) marked as rGO/MnO@C. The materials were characterized by SEM, XRD, FTIR and XPS. Based on this composite, a novel sensor was constructed on a glassy carbon substrate, which exhibited good electrocatalytic activities to the redox reactions of catechol (CC) and hydroquinone (HQ), enabling simultaneous detection of both analytes. Under optimized conditions, the electrochemical sensor demonstrated a linear range of 0.50–90.00 μM for both CC and HQ detection, with respective detection limits of 0.05 μM and 0.03 μM. Moreover, the sensor exhibited excellent sensitivity, selectivity and accuracy for detecting CC and HQ simultaneous in real samples.

MnO/TiO2/C/N-CNTs derived from Mn-doped Ti MOFs for simultaneous detection of catechol and hydroquinone.

Mn-doped Ti-based MOFs (MnTi MOFs) were synthesized by a solvothermal method, and calcined at high temperature after being mixed with pre-prepared PPy nanotubes to give MnO/TiO2/C/N-CNTs composites. The composites were studied by SEM, XRD, XPS and FTIR. Based on these composites, a new electrochemical sensor was prepared, which has good electrocatalytic ability for the redox of catechol (CC) and hydroquinone (HQ), and can detect CC and HQ simultaneously. The results showed that the oxidation peak current of CC and HQ increased linearly in the concentration range of 0.50-120.00 μM. The detection limits were 0.033 μM and 0.019 μM, respectively. The constructed sensor has been successfully used for the simultaneous detection of CC and HQ in lake water and tap water, and has a good recovery rate.

A bimetallic PtAu-modified carbon fiber electrochemical sensor for simultaneous and highly sensitive detection of catechol and hydroquinone in environmental water.

In this study, we report the development of a novel electrochemical sensor capable of the simultaneous detection of catechol (CC) and hydroquinone (HQ) through differential pulse voltammetry. The sensor is constructed using carbon fiber (CF) that has been intricately modified with bimetallic PtAu nanoparticles. The fabrication process involves subjecting CF to ultrasound treatment in an acidic mixture, resulting in the formation of activated carbon fiber (ACF). This activation step not only enhances surface roughness but also facilitates subsequent modification, ensuring the stability of the material. Bimetallic PtAu nanoparticles are then uniformly deposited onto the ACF surface through co-deposition from a metal precursor solution. The modified ACF, adorned with bimetallic PtAu nanoparticles, exhibits excellent conductivity and efficiently catalyzes both CC and HQ in a 10 mM phosphate-buffered saline solution at pH 7.0, thereby enabling their simultaneous detection. Under optimized experimental conditions, this electrochemical sensor achieves impressive detection limits of 0.019 μM for CC and 0.28 μM for HQ within the same concentration range of 0.5-50 μM, respectively. The practicality of the sensor is further demonstrated through recovery experiments using real water samples. This electrochemical sensor, with its superior performance and versatility, shows great potential for applications in analytical chemistry and environmental monitoring.

Distribution and toxicity of dihydroxybenzenes in drinking water sources in Nigeria.

This study provides, for the first time, data on the distribution and toxicity of catechol (CAT) and hydroquinone (HQ) in drinking water sources from Africa. Groundwater (boreholes and hand-dug wells) and surface water in three Southwestern States in Nigeria served as sampling sites. The concentrations of CAT and HQ in groundwater and surface water were determined throughout a period of 12 months, evaluating the effects of seasonal variation (rainy and dry seasons). Mean concentrations of CAT in water samples were higher than those of HQ. In this study, CAT was more frequently detected, with its mean concentration in groundwater samples higher in the rainy season (430 μg L-1) than in the dry season (175 μg L-1). Multivariate analysis using the Principal Component Analysis Software suggests that in most sample sites, CAT and HQ in water samples were from entirely different anthropogenic sources. The most impacted population groups were the toddlers and infants. Similarly, maximum and median concentrations of CAT in water samples pose serious risks to Daphnia at both acute and chronic levels. The results from this study suggest the need for further control of these dihydroxybenzenes through regular monitoring and removal from drinking water during treatment.

Electrochemical sensing performance of two CuO nanomaterial-modified dual-working electrodes.

Two CuO nanostructures, namely, nanospheres (CuONSs) and nanochains (CuONCs) with different shapes but similar diameters, were synthesized and characterized. With these two nanomaterials as electrode modifiers, a systematic comparative study was conducted to examine their electrochemical sensing of catechol (CT) using a dual-working electrode system. The results suggest that for CuONS- and CuONC-modified glassy carbon electrodes, the electrode process for the CT redox is diffusion-controlled, and the modification amount and electrolyte pH have a similar effect on the response. However, the CuONCs showed a higher peak current and lower peak potential, as well as a lower detection limit for the electrochemical oxidation of CT. This is explained by the lower charge transfer impedance and higher electroactive surface area of the CuONCs. Notably, an unexpected peak appeared in the cyclic voltammograms when the pH was <4 for the CuONCs and <3 for the CuONSs. For this phenomenon, UV-Vis spectra, zeta potential, and size distribution experiments demonstrated changes in the two CuO nanostructures at lower pH, illustrating that CuONSs can tolerate a higher pH as compared to CuONCs. The multiple comparisons between the two nanomaterials presented here can provide references for the selection of electrochemical sensing materials.

Scandia-doped zirconia for the electrochemical detection of hazardous dihydroxybenzene (DHB) isomers in water.

In this paper, modified yttria- and scandia-doped zirconium oxide were exploited for the development of an effective electrochemical sensor for the simultaneous detection of dihydroxy benzene (DHB) isomers, i.e. hydroquinone...

Robust anti-impact, energy absorption and thermal properties of polyurethane nanocomposites modified by phenol-amine chemistry

It is still a considerable challenge for polyurethane elastomers (PUE) to possess outstanding mechanical and thermal performance simultaneously against harsh dynamic impact environment due to their heat accumulation, thermal stress softening and mechanical failure. Thus, this article innovatively prepared binary nanofibers composed of carbon nanofiber (CNFs) and aramid nanofibers (ANFs) to reinforce PUE, where catechol (CC) and polyethyleneimine (PEI) were served as interfacial modifier between nanofibers and polymer matrix. PUE with 1.5 wt% binary nanofibers achieve 31.62 % increase in crosslinking density, 146.8 °C improvement in thermal decomposition temperature compared to Neat PUE. Besides, the absorption energy and dynamic compression strength of composites were increased by 40.36 % and 38.26 %, respectively. Because reinforced nanofibers with crosslinking network structures improve the interface interaction between fillers and matrix, facilitate stress transfer and increase the energy threshold of thermal decomposition. The paper supplements the impact resistance analysis of PUE-based protective materials under impact loads, providing a systematic and scientific reference for the design and manufacture of impact resistant materials.

Tweaking the electrocatalytic ability of Cu-MOF by the inclusion of PTA: a selective electrochemical sensor for resorcinol

A facile and superior electrochemical fabrication route was procured to develop the composite of Cu-BTC-MOF/PTA/CFP for the sensitive detection of resorcinol (RL).

Antimicrobial, Anticancer, and Antioxidant Activities of Maize and Clover Pollen Grains Extracts: A Comparative Study with Phytochemical Characterizations.

The failure to treat infectious diseases due to the continual emergence of drug-resistant microbes poses a huge and serious challenge for human health globally. Currently, the discovery and development of natural therapeutic compounds are attracting considerable attention from researchers worldwide. In this project, two types of pollen grains (maize and clover) were evaluated for potential antimicrobial activities. Extracts of both pollen grains were purified using HPLC, which has been shown to have numerous phenolic and flavonoid compounds. Pyro catechol and methyl gallate were detected in high concentrations (1145.56 and 1056.57 µg/mL, respectively) in the maize extract, while caffeic acid, quercetin, and kaempferol (464.73, 393.05, and 390.93 µg/mL, respectively) were among the compounds observed at high concentrations in the clover pollen grains extract. Staphylococcus aureus, Escherichia coli, Salmonella typhi, and Candida albicans were more sensitive to the clover pollen grains extract with inhibition zones of 22 ± 0.2, 18 ± 0.1, 29 ± 0.3, and 42 ± 0.4 mm compared to the size of the inhibitory zones caused by the maize pollen grains extract (19 ± 0.3, 15 ± 0.4, 27 ± 0.1, and 22 ± 0.4 mm, respectively). Moreover, lower MIC values for the clover pollen grains extract were recorded against C. albicans (1.97 ± 0.04 µg/mL), S. aureus (62.5 ± 1.00 µg/mL), and E. coli (62.5 ± 0.07 µg/mL) than the MICs caused by the maize pollen grains extract. The use of a transmission electron microscope revealed that the E. coli that had been treated with the clover pollen grains extract showed changes in its cell walls compared to that treated with the maize pollen grains extract. The clover pollen grains extract exhibited a stronger antioxidant potential, with an IC50 value of 22.18 µg/mL, compared to an IC50 value of 54.85 µg/mL for the maize pollen grains extract, via a DPPH scavenging assay. Regarding anticancer activity, the maize pollen grains extract was revealed to be more effective in terms of inhibiting the human colon cancer cell line HCT-116, with an IC50 value of 67.02 ± 1.37 µg/mL, compared with the observed toxicity caused by the clover extract, with an IC50 value of 75.03 ± 1.02 µg/mL. Overall, the clover pollen grains extract demonstrated potent antibacterial and antioxidant activities, but not anticancer activity, when compared to the maize grains extract. Thus, the current findings related to both types of pollen grains (clover and maize) highlight their potential therapeutic applications for the treatment of certain infectious diseases and malignancies.

An electrochemical sensor based on carbon composites derived from bisbenzimidazole biphenyl coordination polymers for dihydroxybenzene isomers detection.

Co-based coordination polymers (CoCP) based on 4,4'-bis(1H-benzo[d]imidazol-1-yl)-1,1'-biphenyl (BMB) ligand have been synthesized for the first time by the solvothermal method. The CoCP was carbonized at 700 °C under a nitrogen atmosphere to obtain carbide coordination polymer (C-CoCP) with a unique two-dimensional layered network structure. C-CoCP@GO was obtained by binding with GO and C-CoCP, its morphology and structure were investigated by XRD, SEM, EDS, FTIR, and TGA, which confirmed its two-dimensional stacked layered structure with high catalytic activity and large specific surface area. A highly sensitive electrochemical sensor was constructed for the simultaneous detection of hydroquinone and catechol based on the prepared carbon-based composite. Under optimized conditions, the working potentials (vs. Ag/AgCl) of HQ and CC are at 0.097 V and 0.213 V, respectively. The sensor exhibited an extremely wide linear range of 3-600 μM and 3-1750 μM for hydroquinone (HQ) and catechol (CC), respectively, with limits of detection (LOD) of0.46 μM and 0.27 μM. The electrode material demonstrated stability over 14 days without significant attenuation of the response signal. Impressively, the sensor shows highstability, reproducibility, and selectivity due to the stable carbon skeleton structure of the C-CoCP material. In addition, it can be applied to the detection of hydroquinone in real samples with high interference immunity and high recovery. Hence, the C-CoCP@GO composite proved to be a great prospect and highly sensitive sensing platform for the detection of phenolic isomers.

Simultaneous Electrochemical Determination of Hydroquinone and Catechol by Lignocellulose Biopolymers Derived Porous Carbon

AbstractHemicellulose and lignin, which are main components of wood biomass with different structures, were carbonized and activated by KOH to prepare wood biomass‐derived porous carbons (WBM‐PCs). The resulting WBM‐PCs were characterized by SEM, XRD, Raman, FI‐IR, and N2‐adsorption/desorption isotherms, and successfully utilized as an effective modifier on the glassy carbon electrode surface (GCE) for simultaneous electrochemical determination of dihydroxybenzene isomers, i. e. hydroquinone (HQ) and catechol (CC), which are highly toxic and non‐degradable. The resulting WBM‐PCs‐modified GCEs allowed simultaneous determination of HQ and CC with cyclic voltammetry and constant‐potential amperometry. The linear range for determination of HQ by hemicellulose‐derived carbon (HC) was from 1.0 to 3000 μmol/L with the limit of detection (LOD) of 1.05 μmol/L, and that for CC was from 1.0 to 5000 μmol/L with LOD of 0.4 μmol/L. For lignin‐derived carbon (LC), the linear range for HQ was from 0.5 to 1000 μmol/L with LOD of 0.095 μmol/L, and that for CC was from 0.5 to 3000 μmol/L with LOD of 0.15 μmol/L. These results imply that wood biomass (hemicellulose and lignin), which is sustainable, renewable and environment‐friendly material, have potential as an effective precursor of electrochemically active porous carbon materials applicable to various electrochemical sensors.

Efficient metallization based on nondestructive modification of catechol-tetraethylenepentamine composites and electroless deposition applied to polyethylene terephthalate for flexible electronics

An improved metallized polyethylene terephthalate (PET) substrate prepared by catechol (CA) and tetraethylenepentamine (TEPA) composites modification with electroless deposition (ELD) copper layer is presented. Through the polymerization of CA with TEPA, amino and imino groups were generated to adsorb the activated particles required for metallization. To achieve the practical application of this method, different catalytic approaches were validated. Under different catalytic conditions, the catalytic effect of UV light was most pronounced, reaching almost four times than that in darkness. The resulting solid copper layers exhibited highly reliable electrical properties, including a low resistivity of 2.73 μΩ cm, tightly spaced crystalline particles and excellent mechanical properties. The fabricated metallized PET substrates were verified for use in flexible circuit boards, demonstrating the compatibility of the proposed CA-TEPA composites modification method with the PET substrates. This method provides an effective approach to the metallization of the PET substrates, which has a widespread application in manufacturing of flexible electronics such as film capacitors.

Non‐enzymatic electrochemical biosensor based on MgO@rGO‐MoS2 nanohybrid for phenolic compounds detection

In the present work, efforts have been made to fabricate a non‐enzymatic electrochemical biosensor based on MgO nanoparticles modified graphene oxide‐molybdenum disulfide (MgO@rGO‐MoS2) nanohybrid for ultra‐sensitive detection of water‐polluting dihydroxy benzene compound. The one‐pot hydrothermal method has been used to synthesize MgO@rGO‐MoS2 nanohybrid followed by electrophoretic deposition of the nanohybrid onto ITO‐coated glass substrate. The excellent conducting and catalytic ability of MoS2 and MgO facilitates the superior electroanalytical ability of fabricated electrodes, as revealed by the electrochemical studies, whereas the non‐enzymatic approach boosts the stability and sensitivity of the transducing matrix. The fabricated biosensor exhibits linear response in the 0.1 to 200.0 μM concentration range for hydroquinone (Hqn) with a detection limit of 0.086 μM and 0.04 μA μM−1 cm−2 sensitivity. The validation of the biosensor with tap and running river water shows an outstanding recovery rate.