1 / 25

Why diffraction?

Why diffraction?. Learning Outcomes By the end of this section you should: understand what we are looking at with diffraction and why we need diffraction in crystallography be able to compare optical and X-ray diffraction be able to outline the factors which are important in diffraction

simon-tyson
Télécharger la présentation

Why diffraction?

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Why diffraction? Learning Outcomes By the end of this section you should: • understand what we are looking at with diffraction and why we need diffraction in crystallography • be able to compare optical and X-ray diffraction • be able to outline the factors which are important in diffraction • understand the processes of X-ray emission and the basic outline of an X-ray tube

  2. Characterisation of Solids What is it? • Powder • Single crystal • Glass/amorphous • Polymer • Inorganic/Organic • Composite material Insulin crystals, Nasa.gov

  3. Characterisation of Solids What scale are we interested in? • Bulk/Macro – overall structure • Micro (microstructure) – grains, defects • Nano – crystal structure SiC screw disclocation, from http://focus.aps.org/story/v20/st3 Open porous structure in lava flow

  4. Characterisation of Solids What part are we interested in? • Surface vs bulk - • Defects vs “perfection” ---semiconductors Properties? • Mechanical • Magnetic/electronic/ionic • Chemical (e.g. catalytic, pharmaceutical….) Obviously many techniques are required to fully characterise a material Silicon single crystal Graphite surface Pictures from http://materials.usask.ca/photos/

  5. Single crystal Powder diffraction X-ray electron neutron “Perfect Solids” • Best-case scenario? “Perfect” crystalline solid. • Want to find the atom-level structure • Primary techniques: DIFFRACTION

  6. Revisiting Bragg 1912 - Friedrich & Knipping, under direction of Laue Extended by W. H. and W. L. Bragg (father and son) Based on existing optical techniques Max von Laue 1879 -1960 Nobel Prize 1914 “for his discovery of the diffraction of X-rays by crystals” W. H. Bragg 1862 -1942 W. L. Bragg 1890 -1971 Nobel Prize 1915 “for their services in the analysis of crystal structure by means of X-rays"

  7. Optical grating – a 1d analogue Path difference XY between diffracted beams 1 and 2: sin = XY/a  XY = a sin 

  8. Possible Combination of waves • Destructive: Waves combine and are exactly “out of phase” with each other – cancelling.  = /2 • Constructive: Waves combine and are exactly “in phase” with each other – adding together to give maximum possible.  =  • Partial: Somewhere between the two.

  9. Result for OPTICAL grating Path difference XY between diffracted beams 1 and 2: sin = XY/a • XY = a sin  For constructive interference, we want XY to be a whole number of wavelengths So for this set-up, a sin  =  for first order diffraction

  10. Result for OPTICAL grating What we see:

  11. D  L General Diffraction After the diffraction tan  = D/L but if D<<L then we can write sin  ~ D/L But a sin  =  So…. a ~ L/D

  12. Summary of diffraction so far… • Diffraction side: a is related to  Observation side: D is related to L • a sin  =  so sin  = /a • This means that a must be >  or else sin  is > 1 • If a >>  then sin   0 and we see nothing • D is related to 1/a, so the closer the slits, the further apart the diffraction lines. You can see this nicely in this applet: Diffraction Applet

  13. Optical  X-ray • With optical diffraction we can observe effects from a couple of slits • With X-rays, the interaction with matter is very weak – most pass straight through • Therefore we need many (100-1000s) of waves

  14. na 0a D C B A Laue Equations – 3d • By analogy with the above: For constructive interference: (AB – CD) = a (cos na – cos 0a) = nx  and for y & z b (cos nb – cos 0b) = ny  c (cos nc – cos 0c) = nz 

  15. Laue equations – in reality • These work well and describe the interactions • Basic idea is still the constructive interference which occurs at an integer no. of wavelengths • However, not routinely used • Bragg’s law represents a simpler construct for everyday use! 2d sin  = n Make sure you (PX3012) can derive this (Dr. Gibson’s lectures)

  16. But WHY do we need diffraction? Why not just use a big microscope? • “Can’t” focus X-rays (yet?!!) Swift: - Instruments - The X-Ray Telescope • Electron microscope… not quite there yet, limited in application. HREM image of gold Delft University of Technology (2007)

  17. Tilt your head… • If we draw the Bragg construction in the same way as the optical grating, we can clearly see that the diffracted angle is 2. The plane of “reflection” bisects this angle. • Thus we measure 2 in the experiment – next section… “Reflecting plane”   

  18. c =  X-rays and solids X-rays - electromagnetic waves So X-ray photon has E = h X-ray wavelengths vary from .01 - 10Å; those used in crystallography have frequencies 2 - 6 x 1018 Hz Q. To what wavelength range does this frequency range correspond? max = 1.5 Å min = 0.5 Å

  19. Energy and Wavelength Energy of photons usually measured in keV – why? (Å) Looking for wavelengths of the order of Å  therefore need keV

  20. Production of X-rays

  21. X-ray emission Two processes lead to two forms of X-ray emission: • Electrons stopped by target; kinetic energy converted to X-rays • continuous spectrum of “white” radiation, with cut-off at short  (according to h=½mv2) • Wavelength not characteristic of target • Incident electrons displace inner shell electrons, intershell electron transitions from outer shell to inner shell vacancy. • “line” spectra • Wavelength characteristic of target

  22. X-ray spectrum Mixture of continuous and line

  23. Characteristic wavelengths • Thus, each element (target) has a characteristic wavelength. For copper, the  are: • CuK1 = 1.540 Å • CuK2 = 1.544 Å • CuK = 1.39 Å Typical emission spectrum

  24. Energy transitions Many intershell transitions can occur - the common transitions encountered are: 2p (L) - 1s (K), known as the K line 3p (M) - 1s (K), known as the K line (in fact K is a close doublet, associated with the two spin states of 2p electrons)

  25. Example Copper K X-rays have a wavelength of 1.54 Å and are produced when an electron falls from the L shell to a vacant site in the K shell of a copper atom. Calculate the difference in the energy levels between the K and L shells of copper. E = h  = c/  = (3 x108) / (1.54 x 10-10) = 1.95 x 1018 Hz E = h = 6.626 x 10-34x 1.95 x 1018 = 1.29 x 10-15 J ~ 8 keV ..and vice versa - each transition has its own wavelength.

More Related