A simple electrochemical sensor based on rGO/MoS2/CS modified GCE for highly sensitive detection of Pb(ii) in tobacco leaves

High-performance electrode modification materials play a crucial role in improving the sensitivity of sensor detection in electrochemical determination of heavy metals. In this study, a rGO/MoS₂/CS nanocomposite modified glassy carbon electrode (GCE) was used to construct a sensitive sensor for detecting lead ions in tobacco leaves. The reduced graphene oxide (rGO) was used to increase the conductivity of the sensor, and the nano-flowered MoS₂ could provide a large reaction specific surface area and a certain active site for heavy metal reaction. Chitosan (CS) was used to improve the enrichment ability of heavy metals and increase the electrocatalytic activity of electrode. Thus, an electrochemical sensor with excellent performance in reproducibility, stability and anti-interference ability was established. The stripping behavior of Pb(ii) and the application conditions of the sensor were studied by square wave anodic stripping voltammetry (SWASV). The investigation indicated that the sensor exhibited high detection sensitivity in the range of 0.005–0.05–2.0 μM, and the limit of detection (LOD) was 0.0016 μM. This work can provide a fast and effective method for determination of Pb(ii) in samples with low content, such as tobacco leaves.

High-performance electrode modification materials play a crucial role in improving the sensitivity of sensor detection in electrochemical determination of heavy metals.     

A dopamine electrochemical sensor based on a platinum–silver graphene nanocomposite modified electrode

A platinum–silver graphene (Pt–Ag/Gr) nanocomposite modified electrode was fabricated for the electrochemical detection of dopamine (DA). Electrochemical studies of the Pt–Ag/Gr nanocomposite towards DA detection were performed by cyclic voltammetry (CV) and differential pulse voltammetry (DPV). The CV analysis showed that Pt–Ag/Gr/GCE had enhanced electrocatalytic activity towards DA oxidation due to the synergistic effects between the platinum–silver nanoparticles and graphene. The DPV results showed that the modified sensor demonstrated a linear concentration range between 0.1 and 60 μM with a limit of detection of 0.012 μM. The Pt–Ag/Gr/GCE presented satisfactory results for reproducibility, stability and selectivity. The prepared sensor also showed acceptable recoveries for a real sample study.

A platinum–silver graphene nanocomposite was synthesized and characterized. A nanocomposite modified electrode was fabricated in order to investigate the electrochemical detection of dopamine.     

Highly selective non-enzymatic electrochemical sensor based on a titanium dioxide nanowire–poly(3-aminophenyl boronic acid)–gold nanoparticle ternary nanocomposite

A novel three component (titanium dioxide nanowire (TiO₂ NW), poly(3-aminophenyl boronic acid) (PAPBA) and gold nanoparticles (Au NPs)) based ternary nanocomposite (TNC) (designated as TiO₂ NW/PAPBA–Au TNC) was prepared by a simple two-stage synthetic approach and utilized for the fabrication of a non-enzymatic (enzyme-free) glucose (NEG) sensor. In stage 2, the PAPBA–Au NC was formed by oxidative polymerization of 3-APBA using HAuCl₄ as oxidant on the surface of pre-synthesized TiO₂ NW via electrospinning (stage 1). The formation of PAPBA–Au NC as the shell on the surface of the TiO₂ NW (core) was confirmed by field emission scanning electron microscopy (FE-SEM). Notably, we obtained a good peak to peak separation, and a high peak current for the redox Fe(CN)₆^3−/4− process indicating excellent electron transfer capability at the glassy carbon electrode (GCE)/TiO₂ NW/PAPBA–Au TNC interface. Also, the fabricated TiO₂ NW/PAPBA–Au TNC provides excellent electrocatalytic activity towards glucose detection in neutral (pH = 7.0) phosphate buffer solution. The detection of glucose was monitored using differential pulse voltammetry. The obtained sensitivity and detection limits are superior to many of the TiO₂ based enzymatic and non-enzymatic glucose sensors reported in the literature. Furthermore, the TiO₂ NW/PAPBA–Au TNC sensor is preferred because of its high selectivity to glucose in the presence of co-existing interfering substances and practical application for monitoring glucose in human blood serum samples.

A highly selective and sensitive enzymeless electrochemical glucose sensor was fabricated based on a novel ternary nanocomposite composed of titanium dioxide nanowire, poly(3-aminophenyl boronic acid) and gold nanoparticles.     

Synergistic effect of Co–Ni co-bridging with MoS2 nanosheets for enhanced electrocatalytic hydrogen evolution reactions

The depletion of fossil fuels and associated environmental problems have drawn our attention to renewable energy resources in order to meet the global energy demand. Electrocatalytic hydrogen evolution has been considered a potential energy solution due of its high energy density and environment friendly technology. Herein, we have successfully synthesized a noble-metal-free Co–Ni/MoS₂ nanocomposite for enhanced electrocatalytic hydrogen evolution. The nanocomposite has been well characterized using HRTEM, elemental mapping, XRD, and XPS analysis. The as-synthesized nanocomposite exhibits a much smaller onset potential and better current density than those of Co–MoS₂, Ni–MoS₂ and MoS₂, with a Tafel value of 49 mV dec⁻¹, which is comparable to that of a commercial Pt/C catalyst. The synergistic effect and interfacial interaction of Co–Ni bimetallic nanoparticles enhances the intrinsic modulation in the electronic structure resulting in an improved HER performance. Moreover, the electrochemical impedance spectroscopic results suggest smaller resistance values for the Co–Ni/MoS₂ nanocomposite, compared to those for the charge transfer of bare nanosheets, which increase the faradaic process and in turn enhance the HER kinetics for a better performance. Our as-synthesized Co–Ni/MoS₂ nanocomposite holds great potential for the future synthesis of noble-metal-free catalysts.

A noble-metal-free Co–Ni/MoS₂ nanocomposite was synthesized, which showed enhanced electrocatalytic hydrogen evolution performance.     

Reduced graphene oxide-supported methylene blue nanocomposite as a glucose oxidase-mimetic for electrochemical glucose sensing

In this paper, a hybrid nanocomposite (MB-rGO) was synthesized based on the π–π stacking interactions between methylene blue (MB) and reduced graphene oxide (rGO). The as-synthesized nanocomposite was characterized by SEM, TEM, XRD, FTIR, UV-vis and XPS spectra. UV-vis spectroscopy and electrochemical tests suggested the MB-rGO modified on the electrode exhibited glucose oxidase-mimetic catalytic activity towards glucose, and displayed excellent electrocatalytic performance for electrochemical detection of glucose with a wide linear range from 1.04 to 17.44 mM, a low detection limit of 45.8 μM and a large sensitivity of 13.08 μA mM⁻¹ cm⁻². The proposed glucose sensor also showed high stability, reproducibility and good abilities of anti-interference to dopamine, ascorbic acid and uric acid. Moreover, the modified electrode was used to determine glucose concentration in human blood serum samples with satisfactory results.

A novel electrochemical glucose sensor based on methylene blue-reduced graphene oxide nanocomposite was constructed, and the sensor exhibited good glucose oxidase-mimetic electrocatalytic activity towards glucose and practical applicability.     

Electrochemical investigation and amperometry determination iodate based on ionic liquid/polyoxotungstate/P-doped electrochemically reduced graphene oxide multi-component nanocomposite modified glassy carbon electrode

A novel modified glassy carbon electrode (GCE) was successfully fabricated with a tetra-component nanocomposite consisting of (1,1′-(1,4-butanediyl)dipyridinium) ionic liquid (bdpy), SiW₁₁O₃₉Ni(H₂O) (SiW₁₁Ni) Keggin-type polyoxometalate (POM), and phosphorus-doped electrochemically reduced graphene oxide (P-ERGO) by electrodeposition technique. The (bdpy)SiW₁₁Ni/GO hybrid nanocomposite was synthesized by a one-pot hydrothermal method and characterized by UV-vis absorption, Fourier transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD) analysis, thermogravimetric-differential thermal analysis (TGA/DTA), and transmission electron microscopy (TEM). The morphology, electrochemical performance, and electrocatalysis activity of the nanocomposite modified glassy carbon electrode ((bdpy)SiW₁₁Ni/P-ERGO/GCE) were analyzed by field emission scanning electron microscopy (FE-SEM) coupled with energy-dispersive X-ray spectroscopy (EDS), cyclic voltammetry (CV), square wave voltammetry (SWV), and amperometry, respectively. Under the optimum experimental conditions, the as-prepared sensor showed high sensitivity of 28.1 μA mM⁻¹ and good selectivity for iodate (IO₃⁻) reduction, enabling the detection of IO₃⁻ within a linear range of 10–1600 μmol L⁻¹ (R² = 0.9999) with a limit of detection (LOD) of 0.47 nmol L⁻¹ (S/N = 3). The proposed electrochemical sensor exhibited good reproducibility, and repeatability, high stability, and excellent anti-interference ability, as well as analytical performance in mineral water, tap water, and commercial edible iodized salt which might provide a capable platform for the determination of IO₃⁻.

Constructing a sensitive electrochemical sensor based on (bdpy)SiW₁₁Ni/P-ERGO/GCE for IO₃⁻ detection at the nanomolar level with noticeable selectivity.     

Thiolated poly(aspartic acid)-functionalized two-dimensional MoS2, chitosan and bismuth film as a sensor platform for cadmium ion detection

In this work, a sensitive electrochemical platform for determination of cadmium ions (Cd²⁺) is obtained using thiolated poly(aspartic acid) (TPA)-functionalized MoS₂ as a sensor platform by differential pulse anodic stripping voltammetry (DPASV). The performance of the TPA–MoS₂-modified sensor is systemically studied. It demonstrates that the TPA–MoS₂ nanocomposite modified sensor exhibits superior analytical performance for Cd²⁺ over a linear range from 0.5 μg L⁻¹ to 50 μg L⁻¹, with a detection limit of 0.17 μg L⁻¹. Chitosan is able to form a continuous coating film on the surface of the GC electrode. The good sensing performance of the TPA–MoS₂-modified sensor may be attributed to the following factors: the large surface area of MoS₂ (603 m² g⁻¹), and the abundant thiol groups of TPA. Thus, the TPA–MoS₂-modified sensor proves to be a reliable and environmentally friendly tool for the effective monitoring of Cd²⁺ existing in aquacultural environments.

In this work, a sensitive electrochemical platform for determination of cadmium ions (Cd²⁺) is obtained using thiolated poly(aspartic acid) (TPA)-functionalized MoS₂ as a sensor platform by differential pulse anodic stripping voltammetry (DPASV).     

MoS2 nanosheet mediated ZnO–g-C3N4 nanocomposite as a peroxidase mimic: catalytic activity and application in the colorimetric determination of Hg(ii)

A novel colorimetric sensing platform using the peroxidase mimicking activity of ternary MoS₂-loaded ZnO–g-C₃N₄ nanocomposites (ZnO–g-C₃N₄/MoS₂) has been developed for the determination of Hg(ii) ions over co-existing metal ions. The nanocomposite was prepared using an exfoliation process, and the product was further characterized using SEM, TEM, XRD and FTIR analysis. The ZnO–g-C₃N₄/MoS₂ possesses excellent intrinsic catalytic activity to induce the oxidation of 3,3′,5,5′-tetramethylbenzidine (TMB) in aqueous solution in the presence of H₂O₂ to generate deep blue coloured cation radicals (TMB⁺) which can be viewed with the naked eye and produce absorbance at a wavelength of 652 nm. The addition of a well known bioradical scavenger, glutathione (GSH), to the solution hinders the generation of cation radicals and turns the solution colourless. The introduction of Hg(ii) to this solution brings the blue colour back into it, due to the strong affinity of the thiol in the GSH. Based on this mechanism, we have developed a simple and rapid colorimetric sensor for the highly sensitive and selective detection of Hg(ii) ions in aqueous solution with a low detection limit of 1.9 nM. Furthermore, the prepared colorimetric sensor was effectively applied for the quantification analysis of real water samples.

A novel colorimetric sensing platform using the peroxidase mimicking activity of ternary MoS₂-loaded ZnO–g-C₃N₄ nanocomposites (ZnO–g-C₃N₄/MoS₂) has been developed for the determination of Hg(ii) ions over co-existing metal ions.     

Enzyme-less amperometric sensor manufactured using a Nafion–LaNiO3 nanocomposite for hydrogen peroxide

In the present study, an enzyme-less amperometric sensor based on Nafion (NF) and a LaNiO₃ (LNO) nanocomposite was constructed for H₂O₂ detection. LNO from the perovskite group was mixed with NF as an effective solubilizing and stabilizing agent that was used as a novel modifier for modification of the glassy carbon electrode (GCE). The designed sensor showed a desirable electrocatalytic response toward H₂O₂ reduction. The calibration curve revealed two linear portions in the concentration ranges of 0.2–50 μM and 50–3240 μM, and the detection limit was 0.035 μM. The accuracy of the interference-free sensor was checked by recovery analysis in serum samples.

In the present study, an enzyme-less amperometric sensor based on Nafion (NF) and a LaNiO₃ (LNO) nanocomposite was constructed for H₂O₂ detection.     

Shape controllable MoS2 nanocrystals prepared by the single precursor route for electrocatalytic hydrogen evolution

MoS₂ has attracted great attention as a prospective electrocatalyst for generating hydrogen via water electrolysis due to its abundant and inexpensive sources. However, bulk MoS₂ has weak electrocatalytic activity because of its low electrical conductivity and few edge-active sites. Controllable synthesis of MoS₂ with ultrasmall size or complex morphology may be an available strategy to boost its conductivity and edge-active sites. Herein, a facile single-precursor strategy was developed to prepare nanoscale MoS₂ with various morphologies, including quantum dots, nanorods, nanoribbons, and nanosheets. In-depth studies show that the formation of MoS₂ with various shapes is determined by both kinetic and thermodynamic factors such as reaction time and temperature. Electrocatalytic tests reveal that MoS₂ quantum dots have high electrocatalytic performance with a low overpotential of 255 mV and a small Tafel slope of 66 mV dec⁻¹ due to the abundant exposed active edges and excellent intrinsic conductivity.

A facile single-precursor route was designed for the synthesis of shape- and size-controllable MoS₂ nanocrystals, including MoS₂ QDs, nanorods, nanoribbons, and nanosheets. Among them, MoS₂ QDs exhibit higher electrocatalytic activity in HRE.     

A facile one-pot green synthesis of gold nanoparticle-graphene-PEDOT:PSS nanocomposite for selective electrochemical detection of dopamine

A facile one-pot and green method was developed to prepare a nanocomposite of gold nanoparticle (AuNP), graphene (GP) and poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS). Graphene was first electro-exfoliated in a polystyrene sulfonate solution, followed by a one-step simultaneous in situ formation of gold nanoparticle and PEDOT. The as-synthesized aqueous dispersion of AuNP-GP-PEDOT:PSS was thereafter used to modify the glassy carbon electrode (GCE). For the first time, the quaternary composite between AuNP, GP, PEDOT and PSS was used for selective determination of dopamine (DA) and uric acid (UA) in the presence of ascorbic acid (AA). In comparison to a bare GCE, the nanocomposite electrode shows considerably higher electrocatalytic activities toward the oxidation of DA and UA due to a synergistic effect between AuNP, GP, PEDOT and PSS. Using differential pulse voltammetry (DPV), selective determination of DA and UA in the presence of AA could be achieved with a peak potential separation of 110 mV between DA and UA. The sensor exhibits wide linear responses for DA and UA in the ranges of 1 nM to 300 μM and 10 μM to 1 mM with detection limits (S/N = 3) of 100 pM and 10 μM, respectively. Furthermore, the proposed sensor was also successfully used to determine DA in a real pharmaceutical injection sample as well as DA and UA in human serum with satisfactory recovery results.

A facile one-pot green synthesis of gold nanoparticle-graphene-PEDOT:PSS nanocomposite was successfully demonstrated.     

In situ synthesis of MoS2/graphene nanosheets as free-standing and flexible electrode paper for high-efficiency hydrogen evolution reaction

In this article, an exquisite flexible hybrid MoS₂/graphene free-standing electrocatalyst paper was fabricated by a one-step in situ solvothermal process. The assembled MoS₂/graphene catalysts exhibit significantly enhanced electrocatalytic activity and cycling stability towards the splitting of water in acidic solution. Furthermore, a strategic balance of abundant active sites at the edge of the S–Mo–S layers with efficient electron transfer in the MoS₂/graphene hybrid catalyst plays a key role in controlling the electrochemical performance of the MoS₂ nanosheets. Most importantly, the hybrid MoS₂/graphene nanosheet paper shows excellent flexibility and high electrocatalytic performance under the various bending states. This work demonstrates an opportunity for the development of flexible electrocatalysts, which have potential applications in renewable energy conversion and energy storage systems.

An improved flexible hybrid MoS₂/graphene free-standing electrocatalyst paper was fabricated by a one-step in situ solvothermal process for hydrogen evolution reaction applications.     

Fabrication of a polyoxotungstate/metal–organic framework/phosphorus-doped reduced graphene oxide nanohybrid modified glassy carbon electrode by electrochemical reduction and its electrochemical properties

Hybrid nanocomposites based on polyoxometalates (POMs), metal–organic frameworks (MOFs), and graphene oxide (GO) have a unique set of properties. They have specific properties such as high acidity, oxygen-rich surface, and good redox capability from POMs. In contrast, they do not have weaknesses of POMs such as a low surface area, and high solubility in aqueous media. Herein, a novel organic–inorganic nanohybrid compound based on H₃PW₁₂O₄₀ (PW₁₂), a Co-based MOF, and GO was prepared. The prepared hybrid nanocomposite (PW₁₂/MOF/GO) was characterized using different techniques. Then, a PW₁₂/MOF/GO nanocomposite modified glassy carbon electrode (GCE) was fabricated by the drop-casting method and next was dried at room temperature. Then, the PW₁₂/MOF/GO/GCE was subjected to electrochemical reduction at a constant potential of −1.5 V, in 0.1 M H₃PO₄ solution containing 0.10% w/v PW₁₂/MOF/GO additive. The morphology, electrochemical activity, and stability of the modified electrode (PW₁₂/MOF/P@ERGO/GCE) were studied with FE-SEM coupled with EDS, CV, and amperometry. The obtained results confirmed that the PW₁₂/MOF/P@ERGO/GCE could be effective in hydrogen evolution reaction (HER). The electrochemical activity of the PW₁₂/MOF/P@ERGO/GCE due to the desirable microstructure of the electrocatalyst (e.g. high active surface area and homogeneous distribution of the PW₁₂/MOF/P@ERGO), and also the synergistic effect of the blocks, is more than those of PW₁₂/GCE, MOF/GCE, PW₁₂/MOF/GCE, and P@ERGO/GCE. Moreover, the PW₁₂/MOF/P@ERGO/GCE showed an excellent long-term stability under the air atmosphere.

Fabrication of a modified glassy carbon electrode based on a polyoxotungstate/metal–organic framework/phosphorus-doped reduced graphene oxide nanohybrid.     

A study on the tribological property of MoS2/Ti–MoS2/Si multilayer nanocomposite coating deposited by magnetron sputtering

Pure MoS₂ coatings are easily affected by oxygen and water vapor to form MoO₃ and H₂SO₄ which cause a higher friction coefficient and shorter service life. In this work, five kinds of MoS₂/Ti–MoS₂/Si multilayer nanocomposite coatings have been deposited by using unbalanced magnetron sputtering with different modulation period ratios. The tribological tests and nano-indentation experiments have been carried out in order to study the tribological and mechanical properties of the multilayer nanocomposite coating. The results show that the hardness and internal stress of the multilayer nanocomposite coatings are superior to those of the pure MoS₂ coating. The polycrystalline columnar structures are effectively inhibited and the coating densification increases due to the multilayer nanostructure and the doped elements of Ti and Si. The nanocomposite coating with a modulation period ratio of 100 : 100 shows the lowest friction coefficient and wear rate. The multilayer nanocomposite coatings exhibit excellent tribological property under a heavy constant load. Interfaces in multilayer nanostructure coating is able to hinder the dislocations motion and the crack propagation. The doped elements of Ti and Si with nano-multilayer structure enhances the mechanical and tribological properties of MoS₂ coating. This study provides guidelines for optimizing the mechanical and tribological properties of MoS₂ coating.

Pure MoS₂ coatings are easily affected by oxygen and water vapor to form MoO₃ and H₂SO₄ which cause a higher friction coefficient and shorter service life.     

A novel highly selective electrochemical chlorobenzene sensor based on ternary oxide RuO2/ZnO/TiO2 nanocomposites

A novel electrochemical (EC) chlorobenzene (CBZ) sensor was fabricated using a ternary oxide RuO₂/ZnO/TiO₂ nanocomposite (NC)-decorated glassy carbon electrode (GCE). The nanoparticles (NPs) were synthesized by a wet-chemical method and characterized by X-ray photoelectron spectroscopy (XPS), powder X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectroscopy (EDS), and ultraviolet-visible (UV-vis) spectroscopy. The synthesized RuO₂/ZnO/TiO₂ NC was layered as thin film on a GCE with Nafion (5% suspension in ethanol) adhesive, and the as-prepared sensor was subjected to CBZ analysis using an electrochemical approach. The calibration of the proposed CBZ sensor was executed with a linear relation of current versus concentration of CBZs known as the calibration curve. The sensitivity (32.02 μA μM⁻¹ cm⁻²) of the CBZ sensor was calculated from the slope of the calibration curve by considering the active surface area of the GCE (0.0316 cm²). The lower detection limit (LD; 98.70 ± 4.90 pM) was also calculated at a signal-to-noise ratio of 3. Besides these, the response current followed a linear relationship with the concentration of chlorobenzene and the linear dynamic range (LDR) was denoted in the range of 0.1 nM to 1.0 μM. Moreover, the CBZ sensor was found to exhibit good reproducibility, reliability, stability, and fast response time. Finally, the sensing mechanism was also discussed with the energy-band theory of ternary doped semiconductor materials. The sensing activity of the proposed sensor was significantly enhanced due to the combined result of depletion layer formation at the heterojunction of RuO₂/ZnO/TiO₂ NCs as well as the activity of RuO₂ NPs as oxidation catalysts. The proposed CBZ sensor probe based on ternary oxide RuO₂/ZnO/TiO₂ NCs was developed with significant analytical parameters for practical application in monitoring the environmental pollutants of CBZs for the safety of environmental fields on a large scale.

A novel electrochemical (EC) chlorobenzene (CBZ) sensor was fabricated using a ternary oxide RuO₂/ZnO/TiO₂ nanocomposite (NC)-decorated glassy carbon electrode (GCE).     

A novel,highly sensitive electrochemical 1,4-dioxane sensor based on reduced graphene oxide–curcumin nanocomposite

1,4-Dioxane is a carcinogenic, non-biodegradable, organic water pollutant which is used as a solvent in various industries. It is also formed as an undesired by-product in the cosmetic and pharmaceutical industry. Given its carcinogenicity and ability to pollute, it is desirable to develop a sensitive and selective sensor to detect it in drinking water and other water bodies. Current works on this sensor are very few and involve complex metal oxide composite systems. A sensitive electrochemical sensor for 1,4-dioxane was developed by modifying a glassy carbon electrode (GCE) with a reduced graphene oxide–curcumin (rGO–CM) nanocomposite synthesized by a simple solution approach. The prepared rGO–CM was characterized by X-ray Diffraction (XRD), Fourier Transform Infrared (FTIR) Spectroscopy, Raman spectroscopy, UV-Vis spectroscopy, and Scanning Electron Microscopy (SEM). The rGO–CM/GCE sensor was employed for the detection of 1,4-dioxane in the range of 0.1–100 μM. Although, the detection range is narrower compared to reported literature, the sensitivity obtained for the proposed sensor is far superior. Moreover, the limit of detection (0.13 μM) is lower than the dioxane detection target defined by the World Health Organization (0.56 μM). The proposed rGO–CM/GCE also showed excellent stability and good recovery values in real sample (tap water and drinking water) analysis.

Reduced graphene oxide–curcumin (rGO–CM) nanocomposite was prepared from graphite oxide using curcumin. The rGO–CM/GCE was used for highly sensitive 1,4-dioxane detection. The LOD obtained (0.13 μM) was lower than the WHO guideline value.     

Enhanced electrochemical performance of MoS2/graphene nanosheet nanocomposites

Molybdenum disulfide (MoS₂) is attractive as an anode material for next-generation batteries, because of its layered structure being favorable for the insertion/deinsertion of Li⁺ ions, and its fairly high theoretical capacity. However, since the MoS₂ anode material has exhibited disadvantages, such as low electrical conductivity and poor cycling stability, to improve the electrochemical performance of MoS₂ in this study, a nanocomposite structure consisting of MoS₂ and GNS (MoS₂/GNS) as an anode for LIBs was prepared, by controlling the weight ratios of MoS₂/GNS. The X-ray diffraction patterns and electron microscopic analysis showed that the nanocomposite electrode structure consisted of well-formed MoS₂ nanoparticles and GNS. Compared to MoS₂-only, the MoS₂/GNS composites exhibited high retention and improved capacity at high current densities. In particular, among these nanocomposite samples, MoS₂/GNS(8 : 2) with an appropriate portion of GNS exhibited the best LIB performance, due to the lowest interfacial resistance and highest Li-ion diffusivity.

MoS₂/GNS 8 : 2 with an appropriate portion of GNS exhibited the best LIB performance, due to the lowest interfacial resistance and highest Li-ion diffusivity.     

A novel electrochemical sensor for glucose detection based on a Ti3C2Tx/ZIF-67 nanocomposite

A Ti₃C₂T_x/ZIF-67 nanocomposite with outstanding conductivity has been prepared by loading ZIF-67 onto a two-dimensional Ti₃C₂T_x nanosheet. Ti₃C₂T_x sheets were synthesized by etching Ti₃AlC₂, and then ZIF-67 was grown in situ on the Ti₃C₂T_x nanosheet. The Ti₃C₂T_x/ZIF-67 nanocomposite exhibits excellent detection performance for glucose, with a low LOD of 3.81 μM and wide linear detection range of 5–7500 μM. This terrific result is contributed by the synergistic effect of the high electrically conductive ability of Ti₃C₂T_x and active catalytic performance of ZIF-67. Moreover, the electrochemical sensor prepared using the Ti₃C₂T_x/ZIF-67 nanocomposite also shows excellent selectivity, stability and repeatability for glucose detection. The Ti₃C₂T_x/ZIF-67 nanocomposite with outstanding performance has potential applications for electrochemical sensors.

A Ti₃C₂T_x/ZIF-67 nanocomposite with outstanding conductivity has been prepared. The electrochemical sensor based on this nanocomposite exhibits excellent selectivity, stability and repeatability for glucose detection.     

Hybrid ZnO–graphene electrode with palladium nanoparticles on Ni foam and application to self-powered nonenzymatic glucose sensing

A self-powered nonenzymatic glucose sensor electrode boasts the advantages of both a glucose sensor and fuel cell. Herein, an electrode composed of ZnO–graphene hybrid materials on nickel foam (NF) is prepared by electrodeposition of Pd NPs. The electrode is characterized systematically and the dependence of electrocatalytic oxidation of glucose on the concentrations of KOH and glucose, temperature, and potential limit in the anodic direction is investigated. The Pd/NF-ZnO–G electrode shows high catalytic activity, sensitivity, stability, and selectivity in glucose detection, as exemplified by an electrocatalytic glucose oxidation current of 222.2 mA cm⁻² under alkaline conditions, high linearity in the glucose concentration range from 5 μM to 6 mM (R² = 0.98), and high sensitivity of 129.44 μA mM⁻¹⁻¹ cm⁻². The Pd/NF-ZnO–G electrode which exhibits superior electrocatalytic activity under alkaline conditions has large potential in nonenzymatic glucose sensing and direct glucose fuel cells and is suitable for miniaturized self-powered nonenzymatic glucose sensing.

A self-powered nonenzymatic glucose sensor electrode boasts the advantages of both a glucose sensor and fuel cell.     

Mesoporous NiO nanosphere: a sensitive strain sensor for determination of hydrogen peroxide

Exploring the sensitive and reliable methods for the determination of hydrogen peroxide (H₂O₂) is a crucial issue for the health and environmental challenges. Herein, we demonstrate a facile, but rational and effective solvothermal approach to the synthesis of hierarchical NiO mesoporous nanospheres (NiO-MNS) as an effective non-enzymatic sensor towards the H₂O₂ detection. Owing to the intercalation and stabilization effect of polyethylene glycol for the Ni(OH)₂ intermediate, the NiO mesoporous nanosphere (NiO-MNS) product is consistent with the low-dimensional nanostructured NiO blocks with large surface area and plentiful mesopores after the calcination treatment. The obtained NiO-MNS sensor presents superior electrochemical performance with a high sensitivity (236.7 μA mM⁻¹ cm⁻²) and low limit of detection (0.62 μM), as well as the good selectivity and reliability for the further application of H₂O₂ detection. In addition, the unraveling mechanism of the mesopores formation derived from the in situ measurements also offers the valuable guidance for the future design of porous materials for electrochemical devices and other applications.

The NiO mesoporous nanosphere constructing from the low-dimensional nanostructured NiO blocks presents the excellent electrochemical activity for H₂O₂ detection.