Page 401 - Organic Electronics in Sensors and Biotechnology
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378    Chapter  Ten

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               and mixtures of distilled water and methanol.  Films containing long
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               SWCNT bundles are obtained. Andrade et al.  have compared differ-
               ent techniques such as dip-coating, filtration, spray coating, and EPD
               for CNT deposition. The result suggests that dip-coating and EPD pro-
               vide the smoothest CNTs and may be an interesting option for solar
               cell applications, among others.
                   Girishkumar et al.  used EPD to deposit a thin film of SWCNT
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               modified with tetraoctylammonium bromide (TOAB) in tetrahydro-
               furan (THF) on aminopropyltriethoxysilane (APS) coated, optically
               transparent electrodes (OTEs) made of conductive glass. The TOAB
               binds to the surface of the CNT during sonication by hydrophobic
               interactions of its alkyl chain thereby preventing aggregation and set-
               tling of nanotubes. The same group has reported the fabrication of a
               membrane electrode assembly for hydrogen fuel cells by using EPD
               to deposit a SWCNT support and a Pt catalyst on carbon fiber elec-
                     79
               trodes.  Both the electrophoretically deposited nanotubes and plati-
               num retained their nanostructured morphology on the carbon fiber
               surface. Kurnosov et al.  have suggested introducing a resistive
                                     80
               material on top of the conductive cathode to improve the adhesion of
               the CNTs to the substrate and the uniformity of the deposited film. A
               suspension of SWCNT in NiCl /isopropyl alcohol was deposited on
                                         2
                                                    48
               an ITO-coated aluminum cathode. Oh et al.  have performed a simi-
               lar experiment in which functionalized SWCNTs are stabilized in
               MgCl /ethanol and are deposited on ITO-coated glass. In both cases,
                    2
               the nanotubes strongly adhere to the ITO coating. The adhesion has
               been attributed to two factors. The first is the interaction between the
               hydrophilic CNT and ITO surface. 48, 81  The second is the presence of
               the charger salt, MgCl , since Mg  ions form hydroxides at the sur-
                                            2+
                                  2
               face of the negative electrodes that assist the interfacial bonding. 81
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               Girishkumar et al.  have introduced APS coating on OTE surface to
               obtain more uniform electrophoretically deposited films of CNTs.
                   Kamat et al.  have extensively investigated the assembly of solu-
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               bilized SWCNTs into linear bundles at a high DC voltage (>100 V)
               and their deposition on OTE at relatively low DC voltage (∼50 V).
               Purified SWCNTs are solubilized by mixing with TOAB in THF. The
               SWCNT films of varying thickness are obtained by adjusting the
               deposition time.  At high DC voltage of >100 V, the CNTs do not
               deposit and become aligned perpendicular to the two electrodes
               (parallel to the field). The influence of electrode separation has been
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               investigated by Kurnosov et al.  They have found that the uniformity
               of field emission depended significantly on the electrode separation.
               The best uniformity is obtained at the lower end of the separations
               tested (0.3 to 1.8 cm). These authors have observed that for larger
               electrode separations, the emission sites are concentrated at the edges
               of the electrodes due to nonuniformity of the electric field.
                   Once a porous CNT coating or film is obtained, EPD can be
               employed to deposit ceramic or metallic nanoparticles with the aim
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