Charge transport rate controlling factors

The presence of alkali metal ions is crucial for the stabilization of excess charge trapped within the nanopartides. Intercalation of metal ions within the nanoparticle thus becomes a limiting factor as the rate of transport of these ions becomes slower in thicker metal oxide films. This in turn controls the rate of coloration and recovery of the electrochromic effects. Limited efforts have also been made to employ mixed Ti02/W03 [145], WO3/V2O5 [146], and WO3/M0O3 [147] systems to enhance the efficiency of electrochromic effects. The beneficial aspect of these nanostructured semiconductor films in electrochromic devices is yet to be explored in a systematic way. 

This raises some important possibilities, which have not escaped the attention of the electroplating community. For example, while metal deposition is conducted in fairly concentrated solutions of the metal being plated, and at current densities well below the mass-transport limit, additives acting as inhibitors for metal deposition are often introduced at concentrations that are several orders of magnitude lower, to ensure that their supply to the surface will be mass-transport limited. In this way, the tendency for increased rate of metal deposition on certain features on the surface, such as protrusions, will be moderated by the faster diffusion of the inhibitor to the very same areas. Furthermore, if deposition occurs in the region of mixed control, which is usually the case, it must be remembered that the relevant roughness factor is quite different for the charge-transfer and the mass-transport processes, and this may well be a function of current density, since the Faradaic resistance is inherently potential dependent. 

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