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Potentiostats. scanning electrochemical microscopy

As described in the introduction, submicrometer disk electrodes are extremely useful to probe local chemical events at the surface of a variety of substrates. However, when an electrode is placed close to a surface, the diffusion layer may extend from the microelectrode to the surface. Under these conditions, the equations developed for semi-infinite linear diffusion are no longer appropriate because the boundary conditions are no longer correct [97]. If the substrate is an insulator, the measured current will be lower than under conditions of semi-infinite linear diffusion, because the microelectrode and substrate both block free diffusion to the electrode. This phenomena is referred to as shielding. On the other hand, if the substrate is a conductor, the current will be enhanced if the couple examined is chemically stable. For example, a species that is reduced at the microelectrode can be oxidized at the conductor and then return to the microelectrode, a process referred to as feedback. This will occur even if the conductor is not electrically connected to a potentiostat, because the potential of the conductor will be the same as that of the solution. Both shielding and feedback are sensitive to the diameter of the insulating material surrounding the microelectrode surface, because this will affect the size and shape of the diffusion layer. When these concepts are taken into account, the use of scanning electrochemical microscopy can provide quantitative results. For example, with the use of a 30-nm conical electrode, diffusion coefficients have been measured inside a polymer film that is itself only 200 nm thick [98]. [Pg.398]

The time range of the electrochemical measurements has been decreased considerably by using more powerful -> potentiostats, circuitry, -> microelectrodes, etc. by pulse techniques, fast -> cyclic voltammetry, -> scanning electrochemical microscopy the 10-6-10-1° s range has become available [iv,v]. The electrochemical techniques have been combined with spectroscopic ones (see -> spectroelectrochemistry) which have successfully been applied for relaxation studies [vi]. For the study of the rate of heterogeneous -> electron transfer processes the ILIT (Indirect Laser Induced Temperature) method has been developed [vi]. It applies a small temperature perturbation, e.g., of 5 K, and the change of the open-circuit potential is followed during the relaxation period. By this method a response function of the order of 1-10 ns has been achieved. [Pg.580]

The scanning electrochemical microscopy (SECM) technique introduced in recent years by Allen Bard is another area where the smallness of the electrode is essential [38]. The principle in SECM is a mobile UME inserted in an electrolyte solution. The UME is normally operated in a potentiostatic manner in an unstirred solution so that the current recorded is controlled solely by the spherical diffusion of the probed substance to the UME. The current can be quantified from Eqs. 48, 49, or 89 as long as the electrode is positioned far from other interfaces. However, if a solid body is present in the electrolyte solution, the diffusion of the substance to the UME is altered. For instance, when the position of the UME is lowered in the z direction, that is, towards the surface of the object, the diffusion will be partially blocked and the current decreases. By monitoring of the current while the electrode is moved in the x-y plane, the topology of the object can be graphed. The spatial resolution is about 0.25 pm. In one investigation carried out by Bard et al, the... [Pg.543]

The quartz crystal nanobalance (QCN) can be combined with practically any electrochemical methods, such as cyclic voltammetry, chronoamperometry, chronocoulometry, potentiostatic, galvanostatic, rotating disc electrode [11], or potentiometric measurements. The EQCN can be further combined with other techniques, e.g., with UV-Vis spectroscopy [12], probe beam deflection (PBD) [13], radiotracer [14], atomic force microscopy (AEM) [15], and scanning electrochemical microscopy (SECM) [16]. The concept and the instrumentation of... [Pg.257]

The time range of the electrochemical measurements has been decreased considerably by using more powerful -> potentiostats, circuitry, -> microelectrodes, etc. by pulse techniques, fast -> cyclic voltammetry, -> scanning electrochemical microscopy the s range... [Pg.580]


See other pages where Potentiostats. scanning electrochemical microscopy is mentioned: [Pg.270]    [Pg.893]    [Pg.834]    [Pg.360]    [Pg.641]    [Pg.198]    [Pg.79]    [Pg.221]    [Pg.152]    [Pg.198]    [Pg.1084]    [Pg.55]    [Pg.230]    [Pg.786]    [Pg.328]    [Pg.641]    [Pg.103]    [Pg.459]    [Pg.1118]    [Pg.812]    [Pg.812]    [Pg.474]    [Pg.1147]    [Pg.4432]    [Pg.100]   
See also in sourсe #XX -- [ Pg.188 ]




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