Enzyme-free ethanol sensor based on electrospun nickel nanoparticle-loaded carbon fiber paste electrode

We have developed a novel nickel nanoparticle-loaded carbon fiber paste (NiCFP) electrode for enzyme-free determination of ethanol. An electrospinning technique was used to prepare the NiCF composite with large amounts of spherical nanoparticles firmly embedded in carbon fibers (CF). In application to electroanalysis of ethanol, the NiCFP electrode exhibited high amperometric response and good operational stability. The calibration curve was linear up to 87.5 mM with a detection limit of 0.25 mM, which is superior to that obtained with other transition metal based electrodes. For detection of ethanol present in liquor samples, the values obtained with the NiCFP electrode were in agreement with the ones declared on the label. The attractive analytical performance and simple preparation method make this novel material promising for the development of effective enzyme-free sensors.     

Determination of explosives based on novel type of sensor using porphyrin functionalized carbon nanotubes

The hydroxide of meso-tetraphenylporphyrin derivatives functionalized carbon nanotubes (CNTs) was fabricated in our research to explore the interaction between porphyrin and explosive. It was turned out that in the formation of grid porphyrin film, carbon nanotubes as a cruciul base materials promoted the electron transfer rate. Most of important, the results also showed that the electrochemical response was enhanced through increasing the number of -OH substitution in porphyrin. Such information provides the platform for a practical strategy for rational design of the sensor of explosives.     

Smart methanol sensor based on silver oxide-doped zinc oxide nanoparticles deposited on microchips

We have prepared calcined silver oxide-doped zinc oxide nanoparticles (NPs) by a hydrothermal method using reducing agents in alkaline medium. The doped NPs were characterized by UV/vis, FTIR, and X-ray photoelectron spectroscopy, and by X-ray powder diffraction and field-emission scanning electron microscopy. The NPs were deposited on microchips to result in a sensor that has a fast response to methanol in the liquid phase. Features include high sensitivity, low-sample volume, reliability, reproducibility, ease of integration, long-term stability, and enhanced electrochemical responses. The calibration plot is linear (r²?=?0.9981) over the 0.25 mmolL^?1 to 0.25 molL^?1 methanol concentration range. The sensitivity is ~7.917 μA cm^?2 mmolL^?2, and the detection limit is 71.0?±?0.5 μmolL^?1 at a signal-to-noise-ratio of 3.

Composite sorbents based on synthetic manganese oxide and carbon fiber

Manganese oxides have been prepared on the surface of carbon fiber by simple methods: coprecipitation of manganese salts of different valence in the presence of fiber as a support or electrodeposition from Mn(II) salt solution on a carbon fiber cathode, in the presence of chitosan including, under oxidation with air oxygen conditions. The obtained samples have been characterized by scanning electron microscopy, X-ray diffraction, and X-ray photoelectron spectroscopy. Sorption properties of the composites toward As(V) have been studied. The relationships between sorption properties, structure, Mn valence, and manganese oxide surface morphology have been discussed.     

Non-enzymatic amperometric hydrogen peroxide sensor using a glassy carbon electrode modified with gold nanoparticles deposited on CVD-grown graphene

A glassy carbon electrode (GCE) was modified with gold nanoparticles (AuNPs) coated on monolayer graphene (AuNP/MG) by direct in situ sputtering of AuNPs on CVD-generated graphene. This process avoids complicated polymer transfer and polymer cleaning processes and affords AuNPs with a clean surface. The monolayer graphene is ductile and well dispersed. The clean surface of the AuNPs renders this sensor superior to GCEs modified with AuNPs on reduced graphene oxide in terms of the amperometric non-enzymatic determination of hydrogen peroxide. The detection limit is 10 nM (S/N = 3) at 0.55 V (vs. SCE), which is lower than that for similar methods, and the response time is as short as 2 s. Another attractive feature of the sensor is its feasibility for large-scale production via CVD and sputtering.

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Graphical abstract Gold nanoparticles deposited onto monolayered graphene generated by chemical vapor deposition (CVD) are used for electrochemical sensing of H₂O₂, with the detection limit of 10 nM (S/N = 3) and response time of less than 2 s.

     

Voltammetric sensor for caffeine based on a glassy carbon electrode modified with Nafion and graphene oxide

A facile, one-step and template-free method has been developed for the electrodeposition of well-dispersed platinum nanoparticles (Pt-NPs) on a glassy carbon electrode. The effects of various inorganic anions and overpotential on the morphologies and dimensions of the final products were investigated. The resulting Pt-NPs show high electrocatalytic activity towards methanol oxidation and are less easily poisoned by carbon monoxide.

Nonenzymatic glucose sensor based on glassy carbon electrode modified with a nanocomposite composed of nickel hydroxide and graphene

We report on a nonenzymatic glucose sensor based on a glassy carbon electrode that was electrochemically modified with a nanocomposite prepared from nickel hydroxide and graphene. Scanning electron microscopy revealed that the nickel hydroxide in the nanocomposite was present in the form of a nanostructure of three-dimensional spheres that were assembled by many densely arranged nanosheets. The electrocatalytic activity of the electrode toward the oxidation of glucose was investigated by chronoamperometry. The current response was linearly related to the glucose concentration in the range from 1 to 10?μM, with a sensitivity of 494?μA?mM^–1?cm^–2 and a correlation coefficient of 0.9990, and a second range (from 10 to 1000?μM with a sensitivity of 328?μA?mM^–1?cm^–2 and a correlation coefficient of 0.9990). The detection limit was 0.6?μM at a signal-to-noise ratio of 3, and the response time was as short as 2?s.

A uric acid sensor based on electrodeposition of nickel hexacyanoferrate nanoparticles on an electrode modified with multi-walled carbon nanotubes

An electrode sensitive to uric acid was prepared by electrodeposition of nickel(II) hexacyanoferrate(III) on the surface of a glassy carbon electrode modified with multi-walled carbon nanotubes. The morphology of the material was characterized by scanning electron microscopy and Fourier transform infrared spectrometry. The modified electrode were characterized via cyclic voltammetry and amperometry (i - t). It exhibited efficient electron transfer ability and a strong and fast (< 3?s) response towards uric acid which is linear in the range from 0.1???M to 18???M, with a lower detection limit of 50 nM (at an S/N ratio of 3). In addition, the electrode exhibited good reproducibility and long-term stability.

Aptamer-based sensor for diclofenac quantification using carbon nanotubes and graphene oxide decorated with magnetic nanomaterials

In this contribution, a novel label-free electrochemical biosensor for diclofenac (DCF) detection was developed using the unique properties of acid-oxidized carbon nanotubes (CNT), graphene oxide (GO), and Fe₃O₄ magnetic nanomaterials. The GO sheets and CNT were interlinked by ultrafine Fe₃O₄ nanoparticles forming three-dimensional (3D) architectures. The characterization of the nanocomposite was studied by scanning electron microscopy (SEM), energy-dispersive X-ray (EDS), and wavelength-dispersive X-ray (WDX) spectroscopy. Initially, aminated detection probe (aptamer) was surface-confined on the CNT/GO/Fe₃O₄ nanocomposite via the covalent amide bonds formed by the carboxyl groups on the CNT/GO and the amino groups on the oligonucleotides at the 5′ end. Our constructed folding-based electrochemical sensor was used for detection of target molecule utilizing structure-switching aptamers. Signaling arose from changes in electron transfer efficiency upon target-induced changes in the conformation of the aptamer probe. These changes were readily monitored using differential pulse voltammetry technique. This sensor exhibited binding affinities ranging from 100 to 1300 pM with a low detection limit of 33 pM.     

Electrochemical tyrosine sensor based on a glassy carbon electrode modified with a nanohybrid made from graphene oxide and multiwalled carbon nanotubes

We report on a glassy carbon electrode that was modified with a composite made from graphene oxide (GO) and multiwalled carbon nanotubes (MWCNT) that enables highly sensitive determination of L-tyrosine. The sensor was characterized by transmission electron microscopy and electrochemical impedance spectroscopy, and its electrochemical properties by cyclic voltammetry, chronocoulometry and differential pulse voltammetry. The GO/MWCNT hybrid exhibits strong catalytic activity toward the oxidation of L-tyrosine, with a well defined oxidation peak at 761 mV. The respective current serves as the analytical information and is proportional to the L-tyrosine concentration in two ranges of different slope (0.05 to 1.0 μM and 1.0 to 650.0 μM), with limits of detection and quantification as low as 4.4 nM and 14.7 nM, respectively. The method was successfully applied to the analysis of L-tyrosine in human body fluids. The excellent reproducibility, stability, sensitivity and selectivity are believed to be due to the combination of the electrocatalytic properties of both GO and MWCNT. They are making this hybrid electrode a potentially useful electrochemical sensing platform for bioanalysis.

Preparation and characterization of supports with a synthesized layer of catalytic filamentous carbon: III. Synthesis of carbon nanofibers on nickel supported onto aluminum oxide

The synthesis of catalytic filamentous carbon (CFC) on catalysts prepared by supporting Ni²⁺ compounds onto the surface of various alumina modifications (macroporous α-Al₂O₃ and mesoporous ?-Al₂O₃ and δ-Al₂O₃) using two procedures (impregnation and homogeneous precipitation) was studied. The texture characteristics (specific surface area and pore structure) of the parent supports and adsorbents with a CFC layer were compared. The effect of the supporting procedure on the surface morphology of Ni/Al₂O₃ catalysts and the synthesized CFC layer was studied by scanning electron microscopy. It was found that the carbon yield on a macroporous catalyst prepared by homogeneous precipitation was higher than that on a catalyst prepared by impregnation by a factor of ～2. The CFC layer exhibited a mesoporous structure because of a chaotic interlacing of carbon nanofibers, and the synthesis of CFC on macroporous supports resulted in the formation of a bidisperse pore structure of the adsorbent. Active and stable heterogeneous biocatalysts were prepared by the adsorptive immobilization of enzymatically active substances (glucoamylase and nongrowing baker’s yeast cells) on CFC.     

Dopamine sensor based on a glassy carbon electrode modified with a reduced graphene oxide and palladium nanoparticles composite

We report on a sensitive electrochemical sensor for dopamine (DA) based on a glassy carbon electrode that was modified with a nanocomposite containing electrochemically reduced graphene oxide (RGO) and palladium nanoparticles (Pd-NPs). The composite was characterized by scanning electron microscopy, energy dispersive spectroscopy, and electrochemical impendence spectroscopy. The electrode can oxidize DA at lower potential (234 mV vs Ag/AgCl) than electrodes modified with RGO or Pd-NPs only. The response of the sensor to DA is linear in the 1–150 μM concentration range, and the detection limit is 0.233 μM. The sensor was applied to the determination of DA in commercial DA injection solutions.

Sensitive determination of nitric oxide using an electrochemical sensor based on MWCNTs decorated with spherical Au nanoparticles

This paper describes the synthesis, characterisation and application of a very sensitive electrochemical sensor based on a glassy carbon electrode modified with multiwalled carbon nanotubes (MWCNTs) decorated with homogeneously distributed spherical gold nanoparticles (AuNPs). These AuNPs presented diameters ranging from 2 to 10 nm. The AuNPs were prepared directly on the MWCNTs’ surface via a synthesis using HAuCl₄ and citric acid as the reducing agent. The resulting material (Au/MWCNTs) was characterised by scanning electron microscopy (SEM), energy-dispersive X-ray spectrometry (EDX), high-resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD) and Raman spectroscopy. The developed Au/MWCNTs sensor was used in the determination of nitric oxide (NO) in phosphate buffer solution at pH 4.4 by differential pulse voltammetry. In the potential window between 0.5 and 0.65 V, a well-defined oxidation peak was observed, whose height was proportional to the NO concentration in the solution. The Au/MWCNTs-modified electrode exhibited high sensitivity for the determination of nitric oxide, with the limit of detection being 0.21 nmol L^?1 (S/N?=?3). No significant interference was detected for nitrite and CO₂ in the NO detection. Our study demonstrated that the resultant Au/MWCNT-modified electrode can be used for nitric oxide detection in the presence of ascorbic acid, dopamine and uric acid, being potentially useful for determinations of NO in real samples. Figure

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Amperometric determination of L-tyrosine by an enzymeless sensor based on a carbon ceramic electrode modified with copper oxide nanoparticles

We report on the electrochemical formation of copper oxide nanoparticles (CuO-NPs) at a carbon ceramic electrode (CCE) as a highly-porous substrate. A copper film was deposited on the surface of the CCE and derivatized in situ to give CuO-NPs by potential cycling between ?0.8 and 0.35?V in strongly alkaline solution. The electrode was characterized by scanning electron microscopy and cyclic voltammetry. The CuO-NPs exhibited excellent electrocatalytic activity toward the oxidation of L-tyrosine (L-Tyr) in responding linearly in the 2 to 1,350???M concentration range, an associated detection limit (S/N?=?3) of 160?nM, and a sensitivity of 0.61?A?M^?1?cm^?2.

Amperometric nonenzymatic glucose sensor based on a glassy carbon electrode modified with a nanocomposite made from nickel(II) hydroxide nanoplates and carbon nanofibers

We report on a highly sensitive and selective nonenzymatic glucose sensor based on a glassy carbon electrode modified with a composite prepared from nickel(II) hydroxide nanoplates and carbon nanofibers. The nanocomposite was characterized by scanning electron microscopy and powder X-ray diffraction. Electrodes modified with pure Ni(OH)₂ and with the nanocomposite were characterized by electrochemical impedance spectroscopy. Cyclic voltammetric and amperometric methods were used to investigate the catalytic properties of the modified electrodes for glucose electrooxidation in strongly alkaline solution. The sensor exhibits a wide linear range (from 0.001 to 1.2 mM), a low detection limit (0.76 μM), fast response time (< 5 s), high sensitivity (1038.6 μA?·?mM^?1?·?cm^?2), good reproducibility, and long operational stability. Application of the nonenzymatic sensor for monitoring glucose in real samples was also demonstrated.

基于氧化锌/碳纳米纤维材料的氧氟沙星电化学传感器的构建及应用

通过静电纺丝技术合成碳纳米纤维,以循环伏安法在此碳纤维上电聚合乙酸锌制备复合纳米材料作为一种新型的电化学增敏剂,用于修饰玻碳电极,开发了一种基于碳纤维和氧化锌复合材料的新型电化学传感器(ZnO/CNF/GCE)。使用循环伏安法、差分脉冲伏安法等进行电化学催化性能的研究,并优化实验条件。结果表明,与裸电极相比,在pH 5.5磷酸盐缓冲溶液中,ZnO/CNF/GCE修饰电极能使氧氟沙星的峰电流明显提升,线性范围1~200μmol/L,检测限为0.33μmol/L。该ZnO/CNF/GCE修饰电极已用于氧氟沙星滴耳液中氧氟沙星的含量测定。