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Nanotechnology-Enabled Sensors

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7.3 Surface Materials and Surface Modification 397<br />

Fig. 7.23 Polyaniline nanofibres grown by a chemical polymerization technique.<br />

Angelopoulos et al have compared the IR spectra of emeraldine and leucoemeraldine<br />

base polyaniline films (Fig. 7.24). 67,68 They concluded that<br />

the major spectroscopic signatures for polyaniline are generally located between<br />

600 to 1700 cm –1 and 3000 to 3500 cm –1 .<br />

In order to investigate the directionality of polyaniline nanofibres IR<br />

spectroscopy can also be employed. Liu et al 60 showed that for nanofibres<br />

which are aligned to the surface, there is a strong p-polarized peak at<br />

3350 cm –1 which cannot be observed in the bulk polyaniline spectrum.<br />

This peak implies that, in the films that were deposited, the N-H bonds are<br />

nearly perpendicular to the surface.<br />

ICPs posses the ability to change color when their conductivity changes<br />

during a redox process (after interacting with a target analyte) and this<br />

property can be utilized in the fabrication of optical sensors. As can be<br />

seen Fig. 7.25, the UV-visible absorption spectrum of the emeraldine base<br />

polyaniline contains two peaks at approximately 330 nm (3.75 eV) and<br />

650 nm (1.95 eV). The absorption spectra for the pernigraniline base state<br />

show peaks at approximately 280 nm (4.3 eV), 330 nm (3.8 eV) and<br />

530 nm (2.3 eV). For the leucoemeraldine base state only one peak at<br />

340 nm (3.6 eV) is observed. 67 These values change dramatically after the<br />

polyaniline is doped or when it is in nanofibre form.

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