Electrodes pyrolytic

Figure 5 Cyclic voltammograms for trawi -[Ru (16-TMC)02](C104)2 ( 1 mM) in 0.1 M HCIO4 in MeCN. Conditions working electrode, pyrolytic graphite scan rate, 50 mV s. ...

Electrochemical oxidation of natural and synthetic nucleic acids at carbon electrodes pyrolytic graphite [34], paraffin-wax-impregnated spectroscopic graphite [35] and glassy carbon [36, 37] has been studied. It was shown that at pH 4.5 the electrochemical activity of nucleic acids is conditioned by the presence of purine residues in polynucleotide chains. 

In the present work it was studied the dependence of analytical characteristics of the composite SG - polyelectrolyte films obtained by sol-gel technique on the content of non-ionic surfactant in initial sol. Triton X-100 and Tween 20 were examined as surfactants polystyrene sulfonate (PSS), polyvinyl-sulfonic acid (PVSA) or polydimethyl-ammonium chloride (PDMDA) were used as polyelectrolytes. The final films were applied as modificators of glass slides and pyrolytic graphite (PG) electrode surfaces. 

The presence of redox catalysts in the electrode coatings is not essential in the c s cited alx)ve because the entrapped redox species are of sufficient quantity to provide redox conductivity. However, the presence of an additional redox catalyst may be useful to support redox conductivity or when specific chemical redox catalysis is used. An excellent example of the latter is an analytical electrode for the low level detection of alkylating agents using a vitamin 8,2 epoxy polymer on basal plane pyrolytic graphite The preconcentration step involves irreversible oxidative addition of R-X to the Co complex (see Scheme 8, Sect. 4.4). The detection by reductive voltammetry, in a two electron step, releases R that can be protonated in the medium. Simultaneously the original Co complex is restored and the electrode can be re-used. Reproducible relations between preconcentration times as well as R-X concentrations in the test solutions and voltammetric peak currents were established. The detection limit for methyl iodide is in the submicromolar range. 

FIG. 16 Current versus bias voltage for a CdS nanoparticle on the end of an STM tip. The CdS particles were formed by exposing a bilayer of cadmium arachidate on the STM tip to H2S gas. The other conducting surface is a highly oriented pyrolytic graphite electrode. The inset is a plot of differential conductance versus the bias voltage. (Reproduced with permission from Ref. 202. Copyright 1996 National Academy of Sciences, U. S. A.)... 

Figure 1. Reflectance spectra of Fe-TsPc in 0.1 M NaOH adsorbed on the basal plane of a highly ordered pyrolytic graphite (HOPG) electrode at 0.90 V vs. a-Pd and on a Pt electrode at 0.70 V with Ar (0) and O2 ( A ) saturated solutions. Reproduced with...

Figure 17.7 Electrocatalysis of O2 reduction by Pycnoporus cinnabarinus laccase on a 2-aminoanthracene-modified pyrolytic graphite edge (PGE) electrode and an unmodified PGE electrode at 25 °C in sodium citrate buffer (200 mM, pH 4). Red curves were recorded immediately after spotting laccase solution onto the electrode, while black curves were recorded after exchanging the electrochemical cell solution for enzyme-fiiee buffer solution. Insets show the long-term percentage change in limiting current (at 0.44 V vs. SHE) for electrocatalytic O2 reduction by laccase on an unmodified PGE electrode ( ) or a 2-aminoanthracene modified electrode ( ) after storage at 4 °C, and a cartoon representation of the probable route for electron transfer through the anthracene (shown in blue) to the blue Cu center of laccase. Reproduced by permission of The Royal Society of Chemistry fi om Blanford et al., 2007. (See color insert.)...

Anson and co-workers have shown that two Co ions were not necessary for four-electron 02 reduction.266 The mew-substituted complex porphyrin Co(TPyP) (42) complex bears four active pyridyl donors which readily react with four equivalents of [Ru(NH3)5(OH2)]2+ to produce the tetra-ruthenated derivative. The four Ru centers are sufficiently remote that their RuIII/n potentials coincide. Under steady state conditions [Co(TPyP)] Ru(NH3)5 4]8+ (43) adsorbed onto a pyrolytic graphite working electrode catalyzes the reduction of dioxygen (Figure 6). 

Table 1. Linear Ep vs. pH relationships for oxidation of some purines at the stationary pyrolytic graphite electrode...

It has been recently demonstrated that the simplest of the cobalt porphyrins (Co porphine) adsorbed on a pyrolytic graphite electrode is also an efficient electrocatalyst for reduction of 02 into 1120.376 The catalytic activity was attributed to the spontaneous aggregation of the complex on the electrode surface to produce a structure in which the cobalt-cobalt separation is small enough to bridge and activate 02 molecules. The stability of the catalyst is quite poor and largely improved by using porphyrin rings with mew-substitu-tion.377-380 Flowever, as the size of the mew-substituents increases the four-electron reduction efficiency decreases. 

The pores of the silica template can be filled by carbon from a gas or a liquid phase. One may consider an insertion of pyrolytic carbon from the thermal decomposition of propylene or by an aqueous solution of sucrose, which after elimination of water requires a carbonization step at 900°C. The carbon infiltration is followed by the dissolution of silica by HF. The main attribute of template carbons is their well sized pores defined by the wall thickness of the silica matrix. Application of such highly ordered materials allows an exact screening of pores adapted for efficient charging of the electrical double layer. The electrochemical performance of capacitor electrodes prepared from the various template carbons have been determined and are tentatively correlated with their structural and microtextural characteristics. 

A. Salimi, R.G. Compton, and R. Hallaj, Glucose biosensor prepared by glucose oxidase encapsulated sol-gel and carbon-nanotube-modified basal plane pyrolytic graphite electrode. Anal. Biochem. 333, 49— 56 (2004). 

R.R. Moore, C.E. Banks, and R.G. Compton, Basal plane pyrolytic graphite modified electrodes comparison of carbon nanotubes and graphite powder as electrocatalysts. Anal. Chem. 76, 2677—2682... 

Biocompatible nanosized polyamidoamine (PAMAM) dendrimer films provided a suitable microenvironment for heme proteins to transfer electron directly with underlying pyrolytic graphite electrodes. The Mb-PAMAM film can catalytically reduced oxygen, hydrogen peroxide, and nitrite, indicating that the potential applicability of the film can be used to fabricate a new type of biosensor or bioreactor based on the direct electron transfer of Mb [234],... 

X.H. Chen, C.M. Ruan, J.L. Kong, and J.Q. Deng, Characterization of the direct electron transfer and bioelectrocatalysis of horseradish peroxidase in DNA film at pyrolytic graphite electrode. Anal. Chim. 

P. Bianco, A. Taye, and J. Haladjian, Incorporation of cytochrome c and cytochrome c3 within poly(ester-sulfonic acid) films cast on pyrolytic graphite electrodes. J. Electroanal. Chem. 377, 299-303 (1994). 

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