Difference between revisions of "Sample orientation"

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(Reconstruction)
(See Also)
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==See Also==
 
==See Also==
 
* [[Rocking scan]]
 
* [[Rocking scan]]
 +
* [[Example:P3HT orientation analysis]]

Revision as of 08:27, 3 November 2014

For isotropic materials, the orientation of the sample with respect to the beam does not matter. However, for any sample that is anisotropic the sample orientation will strongly influence the scattering pattern. This effect is relevant for any intrinsically anisotropic material, including crystals and aligned bulk materials (liquid crystals, stretched polymers, etc.). Any material which has broken symmetry will also be anisotropic: e.g. a thin film is inherently different along the film normal than in the in-plane direction, and thus is not truly anisotropic.

Anisotropy in the sample is reflected in anisotropy in the reciprocal-space. Thus, the scattering pattern one observes on the detector will depend on the orientation of the sample with respect to the beam.

Reciprocal-space

This is best understood in terms of reciprocal-space. Recall that the signal observed on the detector arises from the intersection of the Ewald sphere with the reciprocal lattice.

Simplified 2D representation of a scattering experiment. The reciprocal-space of a crystal (blue), contains an array of peaks. The only peaks that are observed on the detector are those that intersect the Ewald sphere.

If we reorient the sample, we bring a different set of reciprocal-space peaks into the intersection condition. That is, we bring a different set of crystal planes in the sample into the 'Bragg condition' wherein they give rise to a diffraction peak.

A different sample orientation brings a different set of peaks onto the detector.

Reconstruction

In order to map out the entire reciprocal-space, one can completely rotate the sample, and collection a wide set of images. Adding these images together enables the full 3D reciprocal-space to be reconstructed.


Crystallography anim.gif

See Also