Spectroscopy redox active electrodes

Impedance spectroscopy has been extensively used to follow changes of the interfacial properties of electrodes upon immobilization of enzymes and to characterize biocatalytic processes at enzyme-modified electrodes. Faradaic impedance spectroscopy can be used to study the kinetics of the electron transfer originating from bioelectrocatalytic reactions. It should be noted, that for characterizing redox-active biomolecules by impedance spectroscopy no additional redox probe is added to the electrolyte solution, and the measured electron-transfer process corresponds to the entire bioelectrocatalytic reaction provided by the biocatalyst. Under the condition that the enzyme is not saturated by the substrate, the electron-transfer resistance of the electrode is also controlled by the substrate concentration. Thus, the substrate concentration can be analyzed by the impedance spectroscopy following values [9]. 

Calix[4,6,8]arene derivatives were prepared for the fabrication of SAM redox-active ion, steroids, aromatic amines, metolcarb sensors on Au surfaces. SPR spectroscopy, CV and electrochemical impedance spectroscopy, contact angle measurements were used to monitor guest recognition of the SAM-modified gold electrodes [36-41], Furthermore, multilayering calix[4]resorcinarene was also deposited on ordered Au, quartz and other substrates [42]. 

By the method of introducing Pt into the DLC, the platinum metal is assumed to be distributed over the carbonaceous material bulk as discrete atoms or clusters [154], Essentially, Pt is not a dopant in the DLC, in the sense that the term is used in semiconductor physics. Nor is the percolation threshold surpassed, since the admixture of Pt (not exceeding 15 at. %) did not affect the a-C H resistivity, as was shown by impedance spectroscopy tests p 105 Q, cm, like that of the undoped DLC (see Table 3). It was thus proposed that the Pt effect is purely catalytic one Pt atoms on the DLC surface are the active sites on which adsorption and/or charge transfer is enhanced [75], (And the contact of the carbon matrix to the Pt clusters is entirely ohmic.) This conclusion was corroborated by the studies of Co tetramethylphenyl-porphyrin reaction kinetics at the DLC Pt electrodes [155] redox reactions involving the Co central ion proceed partly under the adsorption of the porphyrin ring on the electrode. 

In this chapter, we review the recent progress in the development of different metal oxide nanoparticles with various shapes and size for fabrication of biosensors. The development of metal oxide nanomaterials surface film for direct electron exchange between electrodes and redox enzymes and proteins will be summarizing. The electrochemical properties, stability and biocatalytic activity of the proposed biosensors will be discussed. The biocompatibility of the metal oxide nanomaterials for enzymes and biomolecules will be evaluated. We will briefly describe some techniques for the investigation of proteins and enzymes when adsorbed to the electrode surfaces. Cyclic voltammetry, impedance spectroscopy, UV-visible spectroscopy and surface imaging techniques were used for surface characterization and bioactivity measuring. 

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