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Electrode Development Chemical Modification of Electrodes Allen J. Bard University of Texas at Austin, Austin, TX 78712 When an electrode, such as a niece of nlatinum or carbon. is dipped into a solution, its &ace becomes covered with a laver of water molecules. Sometimes snecies uresent in the soiution that have been purposely added or are present as imnurities will also attach to the electrode surface. The .. cause the current observed for a given electroche&cal process to be much smaller, because they block access to the electrode surface. Such effects, with electrode surfaces modified by adsorption of species from solution, often accidentally, have been studied extensively by electrochemists for many years. In recent times electrochemists have become interested in purposely modifying an electrode by adsorbing, coating, or attaching specific molecules to the surface. This deliberate and controlled modification of the electrode surface can produce electrodes with new and interesting properties that may form the basis of new applications of electrochemistry and novel devices. Fundamental studies of such modified electrodes have also provided a better insight into the nature of charge transfer and charge transport processes in thin films. In this paper the methods of preparing and characterizing such electrodes are outlined, and several applications are described. More detailed discussions of these touics and the F+re I A Genera resclonschemelorcoolwuintiicnn~wtloi~necctroae sLrtace'o pd.w arnernca.,mwl&electrodt Trerllwnl uxc~znliirnon or metal electrode is treated with y-aminopropyltriethoxysilane.Treatment II: the silanized electrode is treated with compound containing desired group to be anached. R. (8)Structures of some of the compounds mentioned in text. molecule to the surface. One would expect that this technique would also only form a monolayer on the electrode. Fre- quently, however, the silanization reaction causes polymer- ization to take place and thicker layers,equivalent to several monolayers, foim. Polymer Layers. By dipping the electrode into a solution containing a dissolved polymer, e.g., poly(vinylferrocene), and allowingthe solvent to evaporate, one forms a thin (0.1-10pm) film on the surface. A somewhat better method than "dip- coating" for producing more uniform films is "spin-coating" (which is also widelv used in the uroduction of semiconductor chips). Polymer layers can also be produced by electrodepo- sition or by inducing the polymerization of monomers at the electrode surface by electrochemical or other (rf plasma) means. Several t w e s ofuolvmer electrodes have been studied. In some, the poiimer itself is electroactive and can undergo redox reactions. In others the polymer is a polyelectrolyte, that is, a material which contains ionic groups, which can extract charged ions from the solution and hold them by electrostatic binding (e.g., poly(viny1pyridine) or Nafion). How are Modified Electrodes Characterized? After the surface of an electrode has been subjected to one of the above treatments, one must prove that the surface has indeed been modified and find out about the properties and nature of the layer. Since one is dealing with a very small amount of material on the surface, rather sensitive analytical techniques are required. Generally one wants to learn about the amount of material on the surface, how easy it is to oxidize or reduce this material, what is its comnosition and structure. material can he analyzed electrochemically, iince small cur- rents can be measured quite readily and, by Faraday's law, moles of material is equivalent to about 10 microcou- lombs (n = 1).Thus, the cyclic voltammetry of a monolayer of material (Fig. 2) will show a peak with an integrated area equivalent to that amount of material on the electrode surface. growing literature in the field are contained in;eview cle~.',~ How are Electrodes Modified? arti- Modified electrodes can be prepared by several different techniques and are, therefore, often referred to by such names as der~'uatized,polymer-coated, functionalized, and elec- trostatically-bound electrodes. Most frequently the layer or coating on the electrode surface is electroactive, i.e., it can exchange electrons with the underlying substrate material and be oxidized or reduced. althoueh some annlications of none- lectroactive films have also he& discusseb. Strong Chemlsorption. Some species find the surface of the electrode much more hospitable than the hulk solution and so attach spontaneously to the surface. For example organic species, such as those containing douhle bonds, are often hy- drouhobic and stronaly adsorb from aclueous solutions on carbon or platinum sGIfaces. In these cases the amount ad- sorbed on the electrode surface, usually writtenasr,is at most a monolayer, i.e., ahout 1 X 10-lo mol em-=, or 6 X l o J 3mol- ecules Covalent Attachment. Chemical reactions can he carried out to form bonds between the substrate and a molecule of interest (Fig. 1).For example, a metal or carbon can be oxi- dized so that the surface can be considered as consisting of hvdroxvl crouns. Such a surface can be "silanized" bv reaction < 4 t h an organosilane and then reacted with anothe;molecule of interest. In this case the silane is a kind of glue for fixing the ' Murray, R. W., in "Electroanalyiical Chemistry." Bard, A. J., (Editorj, Marcel Dekker, Inc.. New York. Volume 13.1983 (in press). Murray, R. W., Accfs. Chem. Res., 13, 135-141 (1980). 302 Journal of Chemical Education ,. .PDF Image | Chemical Modification of Electrodes
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