Book contents
- Frontmatter
- Contents
- Preface to the First Edition
- Preface to the Second Edition
- 1 The geometry of the crystalline state
- 2 The scattering of X-rays
- 3 Diffraction from a crystal
- 4 The Fourier transform
- 5 Experimental collection of diffraction data
- 6 The factors affecting X-ray intensities
- 7 The determination of space groups
- 8 The determination of crystal structures
- 9 Accuracy and refinement processes
- Physical constants and tables
- Appendices
- Solutions to Problems
- References
- Bibliography
- Index
6 - The factors affecting X-ray intensities
Published online by Cambridge University Press: 11 January 2010
- Frontmatter
- Contents
- Preface to the First Edition
- Preface to the Second Edition
- 1 The geometry of the crystalline state
- 2 The scattering of X-rays
- 3 Diffraction from a crystal
- 4 The Fourier transform
- 5 Experimental collection of diffraction data
- 6 The factors affecting X-ray intensities
- 7 The determination of space groups
- 8 The determination of crystal structures
- 9 Accuracy and refinement processes
- Physical constants and tables
- Appendices
- Solutions to Problems
- References
- Bibliography
- Index
Summary
Diffraction from a rotating crystal
It has been seen that methods of recording X-ray intensities usually involve a crystal rotating in the incident X-ray beam. We shall now look at the problem of determining the total energy in a particular diffracted beam produced during one pass of the crystal through a diffracting position. In order to do this we must make some assumptions about the geometry of the diffraction process; the configuration we shall take is that the crystal is rotating about some axis with a constant angular velocity ω and that the incident and diffracted beams are both perpendicular to the axis of rotation.
Let us first look at the situation when we have a stationary crystal in a diffracting position. Associated with the crystal, and fixed relative to it, there is a reciprocal space within which is defined the Fourier transform, Fx(s), of the electron density of the crystal. For a theoretically perfect crystal of infinite extent the value of Fx(s) would be zero everywhere except at the nodes of a δ-function reciprocal lattice, the weight associated with the point (hkl) being (l/V)Fhkl. However, if the crystal is imperfect in some way there may be non-zero Fx(s) well away from the reciprocal-lattice points and for a finite crystal there will be a small region of appreciable Fx(s) around each of the reciprocal-lattice points. The imperfect-crystal case we shall not consider here but we shall be concerned with the size of the crystal, for this is a factor which must be present in every diffraction experiment.
Consider a crystal completely bathed in an incident beam of intensity Io.
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- An Introduction to X-ray Crystallography , pp. 156 - 189Publisher: Cambridge University PressPrint publication year: 1997