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Introduction to Nanotechnology

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42 METHODS OF MEASURING PROPERTIES<br />

the Debye-Scherrer diffraction results for over 20,000 compounds are available <strong>to</strong><br />

researchers in a JCPDS powder diffraction card file. This method has been widely<br />

used <strong>to</strong> obtain the structures of powders of nanoparticles.<br />

X-ray crystallography is helpful for studying a series of isomorphic crystals, that<br />

is, crystals with the same crystal structure but different lattice constants, such as the<br />

solid solution series Ga,-,In,As or GaAs,-,Sb,, where x can take on the range of<br />

values 0 I x 5 1. For these cubic crystals the lattice constant a will depend on x since<br />

indium (In) is larger than gallium (Ga), and antimony (Sb) is larger than arsenic<br />

(As), as the data in Table B.l indicate. For this case Vegard’s law, Eq. (2.8) of<br />

Section 2.1.4, is a good approximation for estimating the value of a if x is known,<br />

or the value of x if a is known.<br />

3.2.3. Particle Size Determination<br />

In the previous section we discussed determining the sizes of grains in polycrystal-<br />

line materials via X-ray diffraction. These grains can range from nanoparticles with<br />

size distributions such as that sketched in Fig. 3.3 <strong>to</strong> much larger micrometer-sized<br />

particles, held <strong>to</strong>gether tightly <strong>to</strong> form the polycrystalline material. This is the bulk<br />

or clustered grain limit. The opposite limit is that of grains or nanoparticles<br />

dispersed in a matrix so that the distances between them are greater than their<br />

average diameters or dimensions. It is of interest <strong>to</strong> know how <strong>to</strong> measure the sizes,<br />

or ranges of sizes, of these dispersed particles.<br />

The most straightforward way <strong>to</strong> determine the size of a micrometer-sized grain is<br />

<strong>to</strong> look at it in a microscope, and for nanosized particles a transmission electron<br />

microscope (TEM), <strong>to</strong> be discussed in Section 3.3.1, serves this purpose. Figure 3.6<br />

shows a TEM micrograph of polyaniline particles with diameters close <strong>to</strong> l00nm<br />

dispersed in a polymer matrix.<br />

Another method for determining the sizes of particles is by measuring how they<br />

scatter light. The extent of the scattering depends on the relationship between the<br />

particle size d and the wavelength 1 of the light, and it also depends on the<br />

polarization of the incident light beam. For example, the scattering of white light,<br />

which contains wavelengths in the range from 400 nrn for blue <strong>to</strong> 750 nrn for red, off<br />

the nitrogen and oxygen molecules in the atmosphere with respective sizes d = 0.11<br />

and 0.12 nm, explains why the light reflected from the sky during the day appears<br />

blue, and that transmitted by the atmosphere at sunrise and sunset appears red.<br />

Particle size determinations are made using a monochromatic (single-wavelength)<br />

laser beam scattered at a particular angle (usually 90°) for parallel and perpendicular<br />

polarizations. The detected intensities can provide the particle size, the particle<br />

concentration, and the index of refraction. The Rayleigh-Gans theory is used <strong>to</strong><br />

interpret the data for particles with sizes d less than O.lA, which corresponds <strong>to</strong> the<br />

case for nanoparticles measured by optical wavelengths. The example of a laser<br />

beam nanoparticle determination shown in Fig. 3.7 shows an organic solvent<br />

dispersion with sizes ranging from 9 <strong>to</strong> 30 nrn, peaking at 12 nm. This method is<br />

applicable for use with nanoparticles that have diameters above 2 nm, and for smaller<br />

nanoparticles other methods must be used.

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