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Electrocatalytic Activity (electrocatalytic + activity)

Distribution by Scientific Domains
Chemistry74%
Polymers and Materials Science23%

Kinds of Electrocatalytic Activity

  • excellent electrocatalytic activity
    		•
  • high electrocatalytic activity
    		•

    Selected Abstracts

    Preparation, Electrochemistry, and Electrocatalytic Activity of Lead Pentacyanonitrosylferrate Film Immobilized on Carbon Ceramic Electrode

    ELECTROANALYSIS, Issue 21 2008
    H. Razmi
    Abstract Lead pentacyanonitrosylferrate (PbPCNF), a new Prussian blue analog, was immobilized on the surface of a carbon ceramic electrode (CCE) prepared by sol-gel method. The immobilization process consists of adding a certain amount of metallic lead to the electrode matrix before gelation, and chemical derivatization of Pb on the electrode surface to a PbPCNF solid film by immersing the electrode in a solution of sodium pentacyanonitrosylferrate (PCNF). The composition of the synthesized PbPCNF was characterized by FTIR, scanning electron microscopy (SEM), and energy-dispersive X-ray (EDX) techniques. The resulting modified electrode showed electroactivity at two redox centers. The electrochemical behavior of the PbPCNF modified carbon ceramic electrode (PbPCNF|CCE) was studied by cyclic voltammetry. Under optimized conditions the peak-to-peak separation is only 39,mV, indicative of a surface reaction. Ion effects of the supporting electrolyte suggest that cations have a considerable effect on the electrochemical behavior of the modified electrode. The transfer coefficient (,) and the charge transfer rate constant at the modifying film|electrode interface (ks) were calculated. The electrocatalytic activity of the modified electrode toward the electro-reduction of peroxodisulfate was studied in details. [source]

    Retraction: Assembling Interconnected Pt Nanoparticles on Multiwalled Carbon Nanotubes and Their Electrocatalytic Activity for Fuel Cells

    ADVANCED FUNCTIONAL MATERIALS, Issue 9 2010
    Shuangyin Wang
    No abstract is available for this article. [source]

    Retraction: Assembling Interconnected Pt Nanoparticles on Multiwalled Carbon Nanotubes and Their Electrocatalytic Activity for Fuel Cells

    ADVANCED FUNCTIONAL MATERIALS, Issue 9 2010
    Shuangyin Wang
    No abstract is available for this article. [source]

    Aqueous CTAB-Assisted Electrodeposition of Gold Atomic Clusters and Their Oxygen Reduction Electrocatalytic Activity in Acid Solutions,

    ANGEWANDTE CHEMIE, Issue 16 2010
    Chinnaiah Jeyabharathi
    Ein großer Fortschritt: Elektrochemisch synthetisierte, tensidstabilisierte Goldcluster (AuACs; Aun, 5,n,13) katalysieren die elektrochemische Reduktion von Sauerstoff (ORR) in saurer Lösung bei geringen Überpotentialen. Abhängig von der Tensidkonzentration wechselt der Mechanismus der ORR allmählich von einem Vier- zu einem Zweielektronenpfad (siehe Bild; SHE=Standard-Wasserstoffelektrode). Demzufolge verschmelzen die Cluster zu Nanopartikeln. [source]

    Nitrogen-Doped Ordered Mesoporous Graphitic Arrays with High Electrocatalytic Activity for Oxygen Reduction,

    ANGEWANDTE CHEMIE, Issue 14 2010
    Ruili Liu Dr.
    Durch eine metallfreie Prozedur zugänglicher stickstoffdotierter geordneter mesoporöser Graphit (NOMGAs) für die Sauerstoffreduktion (ORR) überzeugt durch eine höhere elektrokatalytische Aktivität als ein käuflicher Pt-C-Katalysator (siehe Diagramm), eine ausgezeichnete Langzeitbeständigkeit und eine Verminderung von Übertrittseffekten. Als Ursache dieser Leistungsfähigkeit werden in die Graphitstruktur integrierte Stickstoffatome diskutiert. [source]

    Composition-Dependent Electrocatalytic Activity of Pt-Cu Nanocube Catalysts for Formic Acid Oxidation,

    ANGEWANDTE CHEMIE, Issue 7 2010
    Dan Xu
    Die Würfel sind gefallen: Die elektrokatalytische Aktivität von Pt- und PtCu-Nanowürfeln unterschiedlicher Zusammensetzung wurde untersucht. Vor allem die Pt80Cu20 -Nanowürfel zeichneten sich durch eine hohe Aktivität und bemerkenswerte Langzeitstabilität in der Ameisensäureoxidation aus. [source]

    High Performance Carbon-Supported Core@Shell PdSn@Pt Electrocatalysts for Oxygen Reduction Reaction

    FUEL CELLS, Issue 4 2010
    W. Zhang
    Abstract In this report, a low-cost and high performance PdSn@Pt/C catalyst with core,shell structure is prepared by two-stage route. X-ray diffraction (XRD) and transmission electron microscopy (TEM) examinations show that the composite catalyst particles distribution is quite homogeneous and has a high surface area and the PdSn@Pt/C catalyst has an average diameter of ca. 5.6,nm. The oxygen reduction reaction (ORR) activity of PdSn@Pt/C was higher than commercial Pt/C catalyst. Catalytic activity is studied by cyclic voltammetry. High electrocatalytic activities could be attributed to the synergistic effect between Pt and PdSn. [source]

    Graphene Based Electrochemical Sensors and Biosensors: A Review

    ELECTROANALYSIS, Issue 10 2010
    Yuyan Shao
    Abstract Graphene, emerging as a true 2-dimensional material, has received increasing attention due to its unique physicochemical properties (high surface area, excellent conductivity, high mechanical strength, and ease of functionalization and mass production). This article selectively reviews recent advances in graphene-based electrochemical sensors and biosensors. In particular, graphene for direct electrochemistry of enzyme, its electrocatalytic activity toward small biomolecules (hydrogen peroxide, NADH, dopamine, etc.), and graphene-based enzyme biosensors have been summarized in more detail; Graphene-based DNA sensing and environmental analysis have been discussed. Future perspectives in this rapidly developing field are also discussed. [source]

    Electrocatalytic Reduction and Determination of Iodate and Periodate at Silicomolybdate-Incorporated-Glutaraldehyde- Cross-Linked Poly- L -lysine Film Electrodes

    ELECTROANALYSIS, Issue 10 2010
    Yu-Ching Pan
    Abstract The present work describes reduction of iodate (IO3,), and periodate (IO4,) at silicomolybdate-doped-glutaraldehyde-cross-linked poly- L -lysine (PLL-GA-SiMo) film coated glassy carbon electrode in 0.1,M H2SO4. In our previous study, we were able to prepare the PLL-GA-SiMo film modified electrode by means of electrostatically trapping SiMo12O404, mediator in the cationic film of PLL-GA, and the voltammetric investigation in pure supporting indicated that the charge transport through the film was fast. Here, the electrocatalytic activity of PLL-GA-SiMo film electrode towards iodate and periodate was tested and subsequently used for analytical determination of these analytes by amperometry. The two electron reduced species of SiMo12O404, anion was responsible for the electrocatalytic reduction of IO3, at PLL-GA-SiMo film electrode while two and six electron reduced species were showed electrocatalytic activity towards IO4, reduction. Under optimized experimental conditions of amperometry, the linear concentration range and sensitivity are 2.5×10,6 to 1.1×10,2,M and 18.47,,A mM,1 for iodate, and 5×10,6 to 1.43×10,4,M and 1014.7,,A mM,1 for periodate, respectively. [source]

    Influence of Metal Nanoparticles on the Electrocatalytic Oxidation of Glucose by Poly(NiIIteta) Modified Electrodes

    ELECTROANALYSIS, Issue 5 2010
    Pratap Azad
    Abstract Conductive polymeric [NiII(teta)]2+ (teta=C-meso-5,5,7,12,12,14-hexamethyl-1,4,8,11-tetra-azacyclotetradecane) films (poly(Ni)) have been deposited on the surface of glassy carbon (GC), Nafion (Nf) modified GC (GC/Nf) and Nf stabilized Ag and Au nanoparticles (NPs) modified GC (GC/Ag-Nf and GC/Au-Nf) electrodes. The cyclic voltammogram of the resulting electrodes, show a well defined redox peak due to oxidation and reduction of poly(Ni) system in 0.1,M NaOH. They show electrocatalytic activity towards the oxidation of glucose. AFM studies reveal the formation of poly(Ni) film on the modified electrodes. Presence of metal NPs increases electron transfer rate and electrocatalytic oxidation current by improving the communication within the Nf and poly(Ni) films. In the presence of metal NPs, 4 fold increase in current for glucose oxidation was observed. [source]

    Platform for Highly Sensitive Alkaline Phosphatase-Based Immunosensors Using 1-Naphthyl Phosphate and an Avidin-Modified Indium Tin Oxide Electrode

    ELECTROANALYSIS, Issue 19 2009
    Abdul Aziz
    Abstract We report a versatile platform for highly sensitive alkaline phosphatase (ALP)-based electrochemical biosensors that uses an avidin-modified indium tin oxide (ITO) electrode as a sensing electrode and 1-naphthyl phosphate (NPP) as an ALP substrate. Almost no electrocatalytic activity of NPP and good electrocatalytic activity of 1-naphthol (ALP product) on the ITO electrodes allow a high signal-to-background ratio. The effective surface covering of avidin on the ITO electrodes allows very low levels of nonspecific binding of proteins to the sensing electrodes. The platform technology is used to detect mouse IgG with a detection limit of 1.0,pg/mL. [source]

    Multiwalled Carbon Nanotubes Encased in Ruthenium Oxide Film as a Hybrid Material for Neurotransmitters Sensor

    ELECTROANALYSIS, Issue 16 2009
    Chien-Chieh Ti
    Abstract A hybrid film (MWCNTs-RuOx,nH2O) which contains multiwalled carbon nanotubes (MWCNTs) along with the incorporation of ruthenium oxide (RuOx,nH2O) has been synthesized on glassy carbon electrode (GCE), gold (Au), indium tin oxide (ITO) and screen printed carbon electrode (SPCE) by potentiostatic methods. The presence of MWCNTs in the hybrid film enhances surface coverage concentration (,) of RuOx,nH2O to ,2100%. The surface morphology of the hybrid film deposited on ITO has been studied using scanning electron microscopy and atomic force microscopy. These two techniques reveal that the RuOx,nH2O incorporated on MWCNTs. Electrochemical quartz crystal microbalance study too reveals the incorporation of MWCNTs and RuOx,nH2O. The MWCNTs-RuOx,nH2O hybrid film exhibits promising enhanced electrocatalytic activity towards the biochemical compounds such as epinephrine and norepinephrine. The electrocatalytic responses of these analytes at RuOx,nH2O, MWCNTs and MWCNTs-RuOx,nH2O hybrid films have been measured using cyclic voltammetry. The obtained sensitivity values from electrocatalysis studies of analytes for MWCNTs-RuOx,nH2O hybrid film are higher than the RuOx,nH2O and MWCNTs films. Finally, the flow injection analysis has been used for the amperometric studies of analytes at MWCNTs-RuOx,nH2O hybrid film modified SPCEs. [source]

    Electrodeposited Silver Nanoparticles on Carbon Ionic Liquid Electrode for Electrocatalytic Sensing of Hydrogen Peroxide

    ELECTROANALYSIS, Issue 13 2009
    Afsaneh Safavi
    Abstract Silver nanoparticles (narrowly dispersed in diameter) were electrodeposited on carbon ionic liquid electrode (CILE) surface using a two-step potentiostatic method. Potentiostatic double pulse technique was used as a suitable and simple method for controlling the size and morphologies of silver nanoparticles electrodeposited on CILE. The obtained silver nanoparticles deposited on CILE surface showed excellent electrocatalytic activity (low overpotential of ,0.35,V vs. Ag/AgCl) towards reduction of hydrogen peroxide. A linear dynamic range of 2,200,,M with an experimental detection limit of 0.7,,M (S/N=3) and reproducibility of 4.1% (n=5) make the constructed sensor suitable for peroxide determination in aqueous solutions. [source]

    Preparation and Characterization of a Tin Pentacyanonitrosylferrate-Modified Carbon Ceramic Electrode: Application to Electrocatalytic Oxidation and Amperometric Detection of L -Cysteine

    ELECTROANALYSIS, Issue 7 2009
    H. Razmi
    Abstract The sol-gel technique was used to construct tin pentacyanonitrosylferrate (SnPCNF) modified composite carbon ceramic electrode (CCE). This involves two steps: construction of CCE containing metallic Sn powder and then electrochemical creating of SnPCNF on the surface of CCE. The SnPCNF modified CCE (SnPCNFlCCE) was characterized by energy-dispersive X-ray (EDX), FTIR and cyclic voltammetry (CV) techniques. The SnPCNF film showed electrocatalytic activity toward the oxidation of L -cysteine. A linear calibration plot was obtained over the L -cysteine concentration range 1,51,,M using chronoamperometry. L -cysteine was determined amperometrically at the surface of this modified electrode. The detection limit (for a signal to noise of 3) and sensitivity were found to be 0.62,,M and 126,,A/mM, respectively. [source]

    Electrocatalytic and Analytical Response of Cobalt Phthalocyanine Modified Carbon Paste Electrodes Towards Antimalarial Endoperoxide Artemisinin

    ELECTROANALYSIS, Issue 3-5 2009
    Chhanda Debnath
    Abstract A cobalt phthalocyanine modified carbon paste electrode was constructed for the analysis of artemisinin in Artemisia annua plant. Artemisinin, a sesquiterpene endoperoxide, is a novel, important antimalarial drug and is used in the therapy against Plasmodium falciparum. The developed cobalt phthalocyanine modified electrode exhibited a significant electrocatalytic activity in presence of artemisinin when using cyclic and differential pulse voltammetry. Under optimized conditions in phosphate buffer of pH,7 a well defined voltammetric peak appeared at about ,500,mV vs. Ag/AgCl. The differential pulse voltammetric peak current of artemisinin was increased linearly with the concentration range of 2.1×10,5 to 5.3×10,4 M (R=0.9997). The limit of detection (LOD) was found to be 6.5×10,6 M. The modified electrode was successfully tested for detecting artemisinin in complex plant materials. [source]

    Multilayer Assembly of Hemoglobin and Colloidal Gold Nanoparticles on Multiwall Carbon Nanotubes/Chitosan Composite for Detecting Hydrogen Peroxide

    ELECTROANALYSIS, Issue 19 2008
    Shihong Chen
    Abstract Chitosan (CS) was chosen for dispersing multi-wall carbon nanotubes (MWNTs) to form a stable CS-MWNTs composite, which was first coated on the surface of a glassy carbon electrode to provide a containing amino groups interface for assembling colloidal gold nanoparticles (GNPs), followed by the adsorption of hemoglobin (Hb). Repeating the assembly step of GNPs and Hb resulted in {Hb/GNPs}n multilayers. The assembly of GNPs onto CS-MWNTs composites was confirmed by transmission electron microscopy. The consecutive growth of {Hb/GNPs}n multilayers was confirmed by cyclic voltammetry and UV-vis absorption spectroscopy. The resulting system brings a new platform for electrochemical devices by using the synergistic action of the electrocatalytic activity of GNPs and MWNTs. The resulting biosensor displays an excellent electrocatalytic activity and rapid response for hydrogen peroxide. The linear range for the determination of H2O2 was from 5.0×10,7 to 2.0×10,3 M with a detection limit of 2.1×10,7 M at 3, and a Michaelis,Menten constant KMapp value of 0.19,mM. [source]

    Glassy Carbon Electrodes Modified with Multiwall Carbon Nanotubes Dispersed in Polylysine

    ELECTROANALYSIS, Issue 15 2008
    Yamile Jalit
    Abstract We report the analytical performance of glassy carbon electrodes (GCE) modified with a dispersion of multiwall carbon nanotubes (MWCNT) in polylysine (Plys) (GCE/MWCNT-Plys). The resulting electrodes show an excellent electrocatalytic activity towards different bioanalytes like ascorbic acid, uric acid and hydrogen peroxide, with important decrease in their oxidation overvoltages. The dispersion of 1.0,mg/mL MWCNT in 1.0,mg/mL polylysine is highly stable, since after 2 weeks the sensitivity for hydrogen peroxide at GCE modified with this dispersion remained in a 90% of the original value. The MWCNT-Plys layer immobilized on glassy carbon electrodes has been also used as a platform to build supramolecular architectures by self-assembling of polyelectrolytes based on the polycationic nature of the polylysine used to disperse the nanotubes. The self-assembling of glucose oxidase has allowed us to obtain a supramolecular multistructure for glucose biosensing. The influence of glucose oxidase concentration and adsorption time as well as the effect of using polylysine or MWCNT-Plys as polycationic layers for further adsorption of GOx is also evaluated. [source]

    Electrochemical Characteristics of Mediated Laccase-Catalysis and Electrochemical Detection of Environmental Pollutants

    ELECTROANALYSIS, Issue 8 2008
    Ying Liu
    Abstract Laccase has been immobilized on the carbon nanotubes modified glassy carbon electrode surface by adsorption. As-prepared laccase retains good electrocatalytic activity to oxygen reduction by using 2,2,-azino-bis-(3-ethylbenzthiazoline-6-sulfonic acid) as the mediator. It can be used as a biosensor for the determination of catechol with broad linear range. Especially, azide, one of inhibitors of laccase, shows sensitive inhibition to catalytic activity of the laccase modified electrode. In addition, the inhibition by fluoride ions has also been studied. These demonstrate that the as-prepared electrode can be used to detect halide and some the toxic pollutants, e.g., catechol and azide based on catalytic or inhibition reaction of laccase. The simple preparation procedure makes the system can be developed as non-inhibition or inhibition biosensor. [source]

    Investigation of the Role of Ionic Liquids in Imparting Electrocatalytic Behavior to Carbon Paste Electrode

    ELECTROANALYSIS, Issue 21 2007
    Norouz Maleki
    Abstract In this paper, a survey has been undertaken to clarify the possible reasons for the electrocatalytic activity obtained by the presence of ionic liquid in carbon paste electrode (CPE). For this purpose, the effect of the addition of traces of ionic liquid to conventional CPE was investigated. Fe(CN)63,/4, was used as a probe and two ionic liquids, namely n -octylpyridinum hexafluorophosphate and 1-octyl-3-methylimidazolium hexaflourophosphate were tested for their electrocatalytic activity. The reasons for this electrocatalytic behavior were evaluated and it was found that different factors such as increase in the ionic conduction of the binder, decrease in the resistance of the modified electrode, increase in ion exchange properties of the electrode and the inherent catalytic activity of ionic liquids are responsible for the considerable improved electrochemical response obtained in the presence of traces of ionic liquid. [source]

    Low Potential Detection of NADH at Titanium-Containing MCM-41,Modified Glassy Carbon Electrode

    ELECTROANALYSIS, Issue 5 2007
    Zhihui Dai
    Abstract Titanium-containing MCM-41 (Ti-MCM-41) modified glassy carbon electrode (GCE) can exhibit an excellent electrocatalytic activity towards the oxidation of ,-Nicotinamide adenine dinucleotide (NADH). A dramatic decrease in the over-voltage of NADH oxidation reaction is observed at 0.28,V (vs. SCE). The modified electrode is found to be stable and reproducible. The electrode shows a linear response for a wide range of 10,1200,,M NADH and the detection limit is 8.0,,M. Ti-MCM-41 mesoporous molecular sieves provide an efficient matrix for development of NADH biosensors and the prepared electrode not only can be used to detect the concentration of NADH in biochemical reaction, but also as the potential matrix of the construction of dehydrogenases biosensor. [source]

    Electrocatalysis and Voltammetric Determination of Dopamine at a Calix[4]arene Crown-4 Ether Modified Glassy Carbon Electrode

    ELECTROANALYSIS, Issue 4 2007
    Guo-Song Lai
    Abstract A sensitive and selective electrochemical method for the determination of dopamine (DA) was developed using a calix[4]arene crown-4 ether (CACE) film modified glassy carbon electrode (GCE). The modified electrode exhibited good electrocatalytic activity for electrochemical oxidation of DA in the pH,6.00 Britton,Robinson buffer solution, and ascorbic acid (AA) did not interfere with it. The diffusion coefficient (D=2.7×10,5,cm2 s,1), and the kinetic parameter such as the electron transfer coefficient (,=0.54) of DA at the surface of CACE were determined using electrochemical approaches. The catalytic oxidation peak currents showed a linear dependence on the DA concentration and a linear analytical curve was obtained in the range of 2.0×10,5,1.0×10,3,M of DA with a correlation coefficient of 0.9990. The detection limit (S/N=3) was estimated to be 3.4×10,6,M. This method was also examined for the determination of DA in an injection sample. In addition, effects of possible interferences were investigated. The present work shows the potential of the proposed method for the fabrication of a modified electrode, as it can be effectively used for voltammetric detection of DA. [source]

    Photoelectrocatalytic Oxidation of NADH with Electropolymerized Toluidine Blue O

    ELECTROANALYSIS, Issue 2-3 2007
    Yusuf Dilgin
    Abstract A poly(Toluidine Blue O) (poly-TBO) modified electrode was successfully prepared by repeated sweeping the applied potential from ,0.6 to +0.8,V (vs. SCE) on a glassy carbon electrode (GCE) in borate buffer solution at pH,9.1,containing 0.1,M NaNO3 and 0.4,mM Toluidine Blue O (TBO). The poly-TBO modified GCE shows electrocatalytic activity toward NADH oxidation in phosphate buffer solution at pH,7.0, with an overpotential of ca. 350,mV lower than that at the bare electrode. The photoelectrocatalytic oxidation of NADH at this electrode was also successfully investigated by using cyclic voltammetry and amperometry at constant potential. When the modified electrode surface was irradiated with a 250,W halogen lamp, a photoelectrocatalytic effect was observed for NADH oxidation and the current was increased about 2.2 times. The applied potential was selected at +100,mV for amperometric and photoamperometric detection of NADH. A linear calibration graph for NADH was obtained in the range between 1.0×10,5 and 1.0×10,3 M and between 5.0×10,6 and 1.0×10,3 M for amperometric and photoamperometric studies, respectively. The effect of some interfering compounds, such as ascorbic acid and dopamine on the electrocatalytic and photoelectrocatalytic oxidation of NADH was tested. [source]

    Copper Oxide , Graphite Composite Electrodes: Application to Nitrite Sensing

    ELECTROANALYSIS, Issue 1 2007
    Biljana, ljuki
    Abstract A simple method for the modification of carbon powder with copper oxides is presented. Carbon powder is impregnated with copper(II) nitrate by stirring carbon powder in copper(II) nitrate solution for 1 hour and subsequently thermally treated at 823,K. The modified carbon powder was characterized using electrochemical and spectroscopic techniques. The existence of both copper(I) and copper(II) oxides have been established. The copper oxide modified carbon powder was used for preparation of composite electrodes, and the electrochemical and electrocatalytic behavior of the resulting composite electrodes was studied. The copper oxide modified carbon powder , epoxy composite electrodes showed a high electrocatalytic activity for the nitrite detection in aqueous media, with the detection limit comparable or lower than detection limits obtained with other electrochemical sensors. [source]

    Adsorptive Stripping Voltammetric Determination of Amitrole at a Multi-Wall Carbon Nanotubes Paste Electdrode

    ELECTROANALYSIS, Issue 5-6 2005
    M. Chicharro
    Abstract This work reports the excellent electrocatalytic activity of carbon nanotubes paste electrodes (CNTPE) prepared by dispersion of multi-wall carbon nanotubes (MWNT) within mineral oil toward the oxidation of 3-amino-1H -1,2,4-triazole (amitrole). The quantification is performed by adsorptive stripping voltammetry (AdSV). The influence of the paste composition and surface pretreatments as well as the amitrole accumulation conditions on the adsorption and further electrooxidation of this herbicide is described. After potentiodynamic pretreatment in 0.050,M phosphate buffer pH,7.4 the amitrole oxidation signal shifts 250,mV toward more negative potential and the sensitivity increases 29 fold, demonstrating that pretreated CNTPEs are extremely useful for a highly sensitive determination of amitrole down to the sub-,M levels. The oxidation peak current is proportional to the amitrole concentration over the range from 0.8 to 7.0,,M (5,min accumulation), with a detection limit of 0.6,,M (48,,gL,1) and a precision of 4.3%, n=20. The proposed method was used for the determination of amitrole in spiked river water (Alberche River (Madrid, Spain)) and tap water samples (Madrid, Spain) at levels higher than 0.6,,M. [source]

    Catalytic Voltammetric Determination of Cladribine in Biological Samples

    ELECTROANALYSIS, Issue 5-6 2003
    Noemí de-los-Santos-Álvarez
    Abstract An electrochemical method for the citotoxic prodrug cladribine determination is proposed. Graphite electrodes modified with cladribine showed a redox process with a formal potential of 0.173,V at pH 6, after the oxidation of the adenine moiety of the drug, whose current can be employed as analytical signal with a detection limit of 75,nM by square-wave voltammetry. As these oxidation products exhibit great electrocatalytic activity toward the electro-oxidation of NADH at low potentials, the analytical response can further be amplified. As a result, the detection limit was improved up to 1,nM using differential pulse voltammetry. The method was applied to the determination of cladribine in serum and urine samples after solid-phase extraction. No electroactive interferences were found in both fluids. The method allows the selective detection of the drug in the presence of the main metabolite, 2-chloroadenosine, which is not able to electrocatalize the NADH oxidation. [source]

    Self-Assembled Graphene,Enzyme Hierarchical Nanostructures for Electrochemical Biosensing

    ADVANCED FUNCTIONAL MATERIALS, Issue 19 2010
    Qiong Zeng
    Abstract The self-assembly of sodium dodecyl benzene sulphonate (SDBS) functionalized graphene sheets (GSs) and horseradish peroxidase (HRP) by electrostatic attraction into novel hierarchical nanostructures in aqueous solution is reported. Data from scanning electron microscopy, high-resolution transmission electron microscopy, and X-ray diffraction demonstrate that the HRP,GSs bionanocomposites feature ordered hierarchical nanostructures with well-dispersed HRP intercalated between the GSs. UV-vis and infrared spectra indicate the native structure of HRP is maintained after the assembly, implying good biocompatibility of SDBS-functionalized GSs. Furthermore, the HRP,GSs composites are utilized for the fabrication of enzyme electrodes (HRP,GSs electrodes). Electrochemical measurements reveal that the resulting HRP,GSs electrodes display high electrocatalytic activity to H2O2 with high sensitivity, wide linear range, low detection limit, and fast amperometric response. These desirable electrochemical performances are attributed to excellent biocompatibility and superb electron transport efficiency of GSs as well as high HRP loading and synergistic catalytic effect of the HRP,GSs bionanocomposites toward H2O2. As graphene can be readily non-covalently functionalized by "designer" aromatic molecules with different electrostatic properties, the proposed self-assembly strategy affords a facile and effective platform for the assembly of various biomolecules into hierarchically ordered bionanocomposites in biosensing and biocatalytic applications. [source]

    Nanoporous Composites: A Three-Dimensional Gold-Decorated Nanoporous Copper Core,Shell Composite for Electrocatalysis and Nonenzymatic Biosensing (Adv. Funct.

    ADVANCED FUNCTIONAL MATERIALS, Issue 14 2010
    Mater.
    M. W. Chen and co-workers present a novel gold-decorated nanoporous copper (Au@NPC) core,shell composite on page 2279. Thin gold shells with controllable thickness are homogeneously deposited onto the internal surfaces of 3D NPC via a spontaneous displacement reaction while NPC is utilized as a reduction agent as well as template and substrate. The inexpensive core shell nanostructure exhibits significant electrocatalytic activity for oxidation methanol and high nonenzymatic sensitivity in detecting glucose. [source]

    A Three-Dimensional Gold-Decorated Nanoporous Copper Core,Shell Composite for Electrocatalysis and Nonenzymatic Biosensing

    ADVANCED FUNCTIONAL MATERIALS, Issue 14 2010
    L.Y. Chen
    Abstract Bimetallic core,shell nanostructures have attracted increasing attention due to their low material costs along with enhanced chemico-physical properties in comparison with their monometallic counterparts. Here, a novel gold-decorated nanoporous copper (Au@NPC) core,shell composite fabricated by a facile in situ hydrometallurgy approach is reported. Thin gold shells with a controllable thickness are homogeneously deposited onto the internal surfaces of 3D nanoporous copper via a spontaneous displacement reaction while nanoporous copper is utilized as a reduction agent as well as 3D template and substrate. The resulting inexpensive core,shell nanostructure exhibits significant electrocatalytic activity for the oxidation of methanol and high non-enzymatic sensitivity in detecting glucose. [source]

    Preparation, Structure, and Electrochemical Properties of Reduced Graphene Sheet Films

    ADVANCED FUNCTIONAL MATERIALS, Issue 17 2009
    Longhua Tang
    Abstract This paper describes the preparation, characterization, and electrochemical properties of reduced graphene sheet films (rGSFs), investigating especially their electrochemical behavior for several redox systems and electrocatalytic properties towards oxygen and some small molecules. The reduced graphene sheets (rGSs) are produced in high yield by a soft chemistry route involving graphite oxidation, ultrasonic exfoliation, and chemical reduction. Transmission electron microscopy (TEM), X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy clearly demonstrate that graphene was successfully synthesized and modified at the surface of a glassy carbon electrode. Several redox species, such as Ru(NH3)63+/2+, Fe(CN)63,/4,, Fe3+/2+ and dopamine, are used to probe the electrochemical properties of these graphene films by using the cyclic voltammetry method. The rGSFs demonstrate fast electron-transfer (ET) kinetics and possess excellent electrocatalytic activity toward oxygen reduction and certain biomolecules. In our opinion, this microstructural and electrochemical information can serve as an important benchmark for graphene-based electrode performances. [source]

    Synthesis of Nanohole-Structured Single-Crystalline Platinum Nanosheets Using Surfactant-Liquid-Crystals and their Electrochemical Characterization

    ADVANCED FUNCTIONAL MATERIALS, Issue 4 2009
    Tsuyoshi Kijima
    Abstract Nanohole-structured single-crystalline Pt nanosheets have been synthesized by the borohydride reduction of Na2PtCl6 confined to the lyotropic liquid crystals (LLCs) of polyoxyethylene (20) sorbitan monooleate (Tween 80) with or without nonaethylene-glycol (C12EO9). The Pt nanosheets of around 4,10,nm in central thickness and up to 500,nm or above in diameter have a number of hexagonal-shaped nanoholes ,1.8,nm wide. High-resolution electron microscope images of the nanosheets showed atomic fringes with a spacing of 0.22,nm indicating that the nanosheets are crystallographically continuous through the nanoholed and non-holed areas. The inner-angle distributions for the hexagonal nanoholes indicate that the six sides of the nanoholes are walled with each two Pt (111), Pt (11) and Pt (010) planes. The formation mechanism of nanoholed Pt nanosheets is discussed on the basis of structural and compositional data for the resulting solids and their precursory LLCs, with the aid of similar nanohole growth observed for a Tween 80 free but oleic acid-incorporated system. It is also demonstrated that the nanoholed Pt nanostructures loaded on carbon exhibit fairly high electrocatalytic activity for oxygen reduction reaction and a high performance as a cathode material for polymer-electrolyte fuel cells, along with their extremely high thermostability revealed through the effect of electron-irradiation. [source]