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after the layer tags are ignored. With the form completely enclosed in the layer, the form can safely be positioned anywhere on the page and all form elements still remain completely active. Although this rule means you can t split one form onto separate layers, you can set up multiple forms on multiple layers and still have them all communicate to one final CGI or other program. This technique uses JavaScript to send the user-input values in the separate forms to hidden fields in the form with the Submit button. Let s say, for example, that you have three separate forms gathering information in three separate layers on a Web page. Call them formA, formB, and formC on layer1, layer2, and layer3, respectively. When the Submit button in formC on layer3 is selected, a JavaScript function is first called by means of an onClick event in the button s <input> tag. The function, in part, looks like the following:



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where u uR juI as before. Some examples of the applications of the theory presented above is given in the following sections.

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Because of the reduced atomic coordination of carbon atoms at the diamond surface, diamond surfaces in vacuum normally undergo a reconstruction to form a -bonded atomic array to restore the normal valence However such surfaces are quite reactive chemically, so tend to react when they come into contact with other phases to lift the reconstruction and form chemisorbed species Because the diamond CVD process involves the use of atomic hydrogen, which forms extremely strong bonds to diamond, CVD diamond is normally completely terminated with chemisorbed hydrogen atoms when it emerges from the reactor, although some more weakly chemisorbed hydrocarbons are sometimes also found on the surface This chemisorbed hydrogen phase is quite stable chemically; in vacuum or an inert atmosphere the diamond has to be heated to temperatures in excess of 800 C in order to desorb it and produce the reconstructed surface.

Although diamond does readily oxidise if heated in air, the hydrogen-terminated surface is kinetically relatively stable in air at room temperature, and even after several hours the hydrogen termination persists On a timescale of weeks however, slow oxidation does take place to replace the hydrogen with chemisorbed oxygen [11] The exact forms in which these oxygen species are bonded to the surface are less well known, but the available evidence would indicate that ether and carbonyl linkages dominate when diamond is in contact with dry oxygen; in the presence of hydrogen or moisture, surface hydroxyl groups are probably present [12] It follows that most as-received diamond electrodes are probably mainly terminated with these various oxygen functionalities Changes in the surface termination, however, undoubtedly occur during electrode usage, which can in uence the electrode performance Detailed studies [eg.

12] of how diamond electrode surfaces that have been freshly hydrogenated in a H plasma are modi ed by the electrochemical environment have been performed Typical XPS spectra are illustrated in Figure 178, which presents the C 1s spectra from diamond surfaces subject to differing treatments The changes in pro le arise from chemical shift effects due to bonding to oxygen If the potential is maintained within the electrochemical window, the hydrogenated surface is quite stable in solution for a period of hours and very little oxygen is observed on the surface after it is withdrawn from solution However, if potentials outside this window are employed then rapid oxidation of the surface occurs It can be seen that anodic treatment of the surface produces a spectrum rather similar to that from oxygen plasma treatment.

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