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Electroanalytical Applications (electroanalytical + application)

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Chemistry100%

Selected Abstracts

Electroanalytical Applications of Microporous Zeolites and Mesoporous (Organo)Silicas: Recent Trends

ELECTROANALYSIS, Issue 7 2008
Alain WalcariusArticle first published online: 10 MAR 200
Abstract Microporous zeolites and ordered mesoporous (organo)silicas have been widely used as electrode modifiers because of their attractive properties (ion exchange and size selectivity of zeolites, well ordered nanoreactors containing a high number of widely accessible active centers in mesoporous (organo)silicas). These properties have been intelligently combined to selected redox processes to improve the response of the resulting modified electrodes or to design novel electrochemical detection schemes. This up-to-date review provides the recent advances made in the electroanalytical applications of zeolite modified electrodes and discusses the interest of ordered mesoporous (organo)silica materials in electroanalysis. [source]

Evaluation of Thin Film Titanium Nitride Electrodes for Electroanalytical Applications

ELECTROANALYSIS, Issue 10 2007
Carolina Nunes, Kirchner
Abstract Titanium nitride is a hard and inert conducting material that has yet not been widely used as electrode material for electroanalytical applications although there are highly developed protocols available to produce well adherent micro and nanostructured electrodes. In this paper the possibilities of using titanium nitride thin films for electroanalytical applications is investigated. Scanning electrochemical microscope (SECM) was used for analysis of the redox kinetics of a selected fast redox couple at thin films of titanium nitride (TiN) in different thicknesses. The investigation was carried out by approaching an amperometric ultramicroelectrode (UME) to the TiN film while the soluble redox couple (ferrocenemethanol/ferrociniummethanol) served as mediator in a SECM configuration. The substrate was biased at a potential so that it rereduces the species being produced at the UME, thus controlling the feedback effect. Normalized current,distance curves were fitted to the theoretical model in order to find the apparent heterogeneous standard rate constant (k°) at the sample. The data are further supported by structural investigation of the TiN films using scanning force microscopy and X-ray photoelectron spectroscopy. It was found that the kinetics are little influenced by prolonged storage in air. The heterogeneous standard rate constants in 2,mM ferrocenemethanol were (0.73±0.05)×10,3,cm s,1 for 20,nm TiN thin layer, (1.5±0.2)×10,3,cm s,1 for 100,nm TiN thin layer and (1.3±0.2)×10,3,cm s,1 for 300,nm TiN thin layer after prolonged storage in air. Oxidative surface treatment (in order to remove organic adsorbates) decreased the kinetics in agreement with a thicker oxide layer on the material. The results suggest that their direct use for amperometric detection of reversible redox systems in particular at miniaturized configurations may be advantageous. [source]

Fabrication, Characterisation and Voltammetric Studies of Gold Amalgam Nanoparticle Modified Electrodes

CHEMPHYSCHEM, Issue 9 2004
Christine M. Welch
Abstract The fabrication, characterisation, and electroanalytical application of gold and gold amalgam nanoparticles on glassy carbon electrodes is examined. Once the deposition parameters for gold nanoparticle electrodes were optimised, the analytical utility of the electrodes was examined in CrIIIelectroanalysis. It was found that gold nanoparticle modified (Au-NM) electrodes possess higher sensitivity than gold macroelectrodes. In addition, gold amalgam nanoparticle modified (AuHg-NM) electrodes were fabricated and characterised. The response of those electrodes was recorded in the presence of important environmental analytes (heavy metal cations). It was found AuHg-NM electrodes demonstrate a unique voltammetric behaviour and can be applied for electroanalysis when enhanced sensitivity is crucial. [source]

Electrochemical Properties of Ordered Mesoporous Carbon Film Adsorbed onto a Self-Assembled Alkanethiol Monolayer on Gold Electrode

ELECTROANALYSIS, Issue 2 2009
Dan Zheng
Abstract A stable ordered mesoporous carbon (OMC) film electrode was successfully constructed by adsorbing OMC onto a self-assembled monolayer (SAM) of C18H37SH chemisorbed on the Au electrode. Transmission electron microscopy (TEM), atomic force microscopy (AFM), and electrochemical methods were used to characterize the properties of the OMC film electrode. The adsorbed OMC can restore the heterogeneous electron transfer almost totally blocked by the alkanethiol monolayer. Nyquist plots show a sharply decrease of the charge transfer resistance (Rct) of the Fe(CN) couple at the OMC film electrode. Furthermore, the OMC film electrode is found to possess a significantly reduced interfacial capacitance and largely enhanced current response of hydrogen peroxide. This novel approach to the fabrication of stable OMC film electrode with excellent electrochemical properties is believed to be very attractive for electrochemical studies and electroanalytical applications. [source]

Electroanalytical Applications of Microporous Zeolites and Mesoporous (Organo)Silicas: Recent Trends

ELECTROANALYSIS, Issue 7 2008
Alain WalcariusArticle first published online: 10 MAR 200
Abstract Microporous zeolites and ordered mesoporous (organo)silicas have been widely used as electrode modifiers because of their attractive properties (ion exchange and size selectivity of zeolites, well ordered nanoreactors containing a high number of widely accessible active centers in mesoporous (organo)silicas). These properties have been intelligently combined to selected redox processes to improve the response of the resulting modified electrodes or to design novel electrochemical detection schemes. This up-to-date review provides the recent advances made in the electroanalytical applications of zeolite modified electrodes and discusses the interest of ordered mesoporous (organo)silica materials in electroanalysis. [source]

Evaluation of Thin Film Titanium Nitride Electrodes for Electroanalytical Applications

ELECTROANALYSIS, Issue 10 2007
Carolina Nunes, Kirchner
Abstract Titanium nitride is a hard and inert conducting material that has yet not been widely used as electrode material for electroanalytical applications although there are highly developed protocols available to produce well adherent micro and nanostructured electrodes. In this paper the possibilities of using titanium nitride thin films for electroanalytical applications is investigated. Scanning electrochemical microscope (SECM) was used for analysis of the redox kinetics of a selected fast redox couple at thin films of titanium nitride (TiN) in different thicknesses. The investigation was carried out by approaching an amperometric ultramicroelectrode (UME) to the TiN film while the soluble redox couple (ferrocenemethanol/ferrociniummethanol) served as mediator in a SECM configuration. The substrate was biased at a potential so that it rereduces the species being produced at the UME, thus controlling the feedback effect. Normalized current,distance curves were fitted to the theoretical model in order to find the apparent heterogeneous standard rate constant (k°) at the sample. The data are further supported by structural investigation of the TiN films using scanning force microscopy and X-ray photoelectron spectroscopy. It was found that the kinetics are little influenced by prolonged storage in air. The heterogeneous standard rate constants in 2,mM ferrocenemethanol were (0.73±0.05)×10,3,cm s,1 for 20,nm TiN thin layer, (1.5±0.2)×10,3,cm s,1 for 100,nm TiN thin layer and (1.3±0.2)×10,3,cm s,1 for 300,nm TiN thin layer after prolonged storage in air. Oxidative surface treatment (in order to remove organic adsorbates) decreased the kinetics in agreement with a thicker oxide layer on the material. The results suggest that their direct use for amperometric detection of reversible redox systems in particular at miniaturized configurations may be advantageous. [source]

Inlaid Multi-Walled Carbon Nanotube Nanoelectrode Arrays for Electroanalysis

ELECTROANALYSIS, Issue 1 2005
Jun Li
Abstract The rapid development in nanomaterials and nanotechnologies has provided many new opportunities for electroanalysis. We review our recent results on the fabrication and electroanalytical applications of nanoelectrode arrays based on vertically aligned multi-walled carbon nanotubes (MWCNTs). A bottom-up approach is demonstrated, which is compatible with Si microfabrication processes. MWCNTs are encapsulated in SiO2 matrix leaving only the very end exposed to form inlaid nanoelectrode arrays. The electrical and electrochemical properties have been characterized, showing well-defined quasireversible nanoelectrode behavior. Ultrasensitive detection of small redox molecules in bulk solutions as well as immobilized at the MWCNT ends is demonstrated. A label-free affinity-based DNA sensor has shown extremely high sensitivity approaching that of fluorescence techniques. This platform can be integrated with microelectronics and microfluidics for fully automated microchips. [source]

The Influence of Doping Levels and Surface Termination on the Electrochemistry of Polycrystalline Diamond

ELECTROANALYSIS, Issue 6 2004
Matthew
Abstract The influence of surface chemistry and boron doping density on the redox chemistry of Fe(CN) at CVD polycrystalline diamond electrodes is considered. It is demonstrated that for this couple both the doping density and the surface chemistry are important in determining the rate of charge transfer at the electrode/electrolyte interface. For hydrogen terminated CVD diamond metallic electrochemical behavior is always observed, even at boron doping densities as low as 7×1018,cm,3. In contrast, the electrochemical behavior of oxygen terminated CVD diamond varies with doping density, a metallic response being observed at high doping density and semiconductor behavior at low doping density. It is shown that the results attained may be explained by a surface state mediated charge transfer mechanism, thus demonstrating the importance of controlling surface chemistry in electroanalytical applications of diamond. [source]