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Introduction to Nanotechnology

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292 ORGANIC COMPOUNDS AND POLYMERS<br />

appearing at wavelengths of 640, 656, and 652nm, respectively, which is the<br />

expected shift <strong>to</strong>ward lower energies (i.e., longer wavelengths) with increasing<br />

particle size.<br />

11.4. POLYMERS<br />

11.4.1. Conductive Polymers<br />

Many nanoparticles are metals, such as the structural magic number particle Au,,.<br />

The metals under consideration in their bulk form are good conduc<strong>to</strong>rs of electricity.<br />

There are also polymers, called conductive polymers or organic metals, which are<br />

good conduc<strong>to</strong>rs of electricity, and polyacetylene is an example. Many polyaniline-<br />

based polymers are close <strong>to</strong> silver in the galvanic series, which lists metals in<br />

the order of their potential or ease of oxidation.<br />

Acetylene HC-CH has the monomer<br />

H H<br />

-c=c-<br />

(11.16)<br />

corresponding <strong>to</strong> the repeat unit [-CH=CH-1,. Other examples of compounds<br />

that produce conducting polymers are the benzene derivative aniline C6H,NH,,<br />

which may also be written 4NH,, and the two 5-membered ring compounds pyrrole<br />

(C4H4NH) and thiophene (C4H4S). The structure of thiophene is sketched in<br />

Fig. 10.20, and pyrrole has the same structure with the sulfur a<strong>to</strong>m S replaced by<br />

a nitrogen a<strong>to</strong>m N bonded <strong>to</strong> a hydrogen H. These molecules all have alternating<br />

double-single chemical bonds, and hence they form polymers that are n-conjugated.<br />

The n conjugation of the carbon bonds along the oriented polymer chains provides<br />

pathways for the flow of conduction electrons, and hence it is responsible for the<br />

good electrical conduction along individual polymer nanoparticles. Polarons, or<br />

electrons surrounded by clouds of phonons, may also contribute <strong>to</strong> this intrinsic<br />

conductivity. The overall conductivity, however, is less than this intrinsic conducti-<br />

vity, and must take in<strong>to</strong> account the particular nature of the polymer.<br />

Wessling (2000) has proposed an explanation of the high electrical conductivity<br />

of conductive polymers such as polyacetylene and polyaniline on the basis of their<br />

nanostructure involving primary particles with a metallic core of diameter 8 nm<br />

surrounded by an amorphous nonconducting layer 0.08nm thick of the same<br />

[CZH2], composition. Figure 11.9 presents a sketch of the model proposed by<br />

Wessling based on scanning electron microscope pictures of conductive polymers.<br />

The individual nanoparticles are seen joined <strong>to</strong>gether in networks comprising 30-50<br />

particles, with branching every 10 or so particles. Several of the nanoparticles are<br />

pictured with their <strong>to</strong>p halves removed <strong>to</strong> display the inner metallic core, and their<br />

surrounding amorphous coating. The electrical conductivity mechanism is purely<br />

metallic within each particle, and involves thermally activated tunneling of the

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