Template:Short description In many areas of science, Bragg's law — also known as Wulff–Bragg's condition or Laue–Bragg interference — is a special case of Laue diffraction that gives the angles for coherent scattering of waves from a large crystal lattice. It describes how the superposition of wave fronts scattered by lattice planes leads to a strict relation between the wavelength and scattering angle. This law was initially formulated for X-rays, but it also applies to all types of matter waves including neutron and electron waves if there are a large number of atoms, as well as to visible light with artificial periodic microscale lattices.

HistoryEdit

File:Diffusion rayleigh et diffraction.svg
X-rays interact with the atoms in a crystal.

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Bragg diffraction (also referred to as the Bragg formulation of X-ray diffraction) was first proposed by Lawrence Bragg and his father, William Henry Bragg, in 1913<ref>Template:Cite journal</ref> after their discovery that crystalline solids produced surprising patterns of reflected X-rays (in contrast to those produced with, for instance, a liquid). They found that these crystals, at certain specific wavelengths and incident angles, produced intense peaks of reflected radiation.

File:Braggs Law2.svg
According to the Template:Math deviation, the phase shift causes constructive (left figure) or destructive (right figure) interferences.

Lawrence Bragg explained this result by modeling the crystal as a set of discrete parallel planes separated by a constant parameter Template:Mvar. He proposed that the incident X-ray radiation would produce a Bragg peak if reflections off the various planes interfered constructively. The interference is constructive when the phase difference between the wave reflected off different atomic planes is a multiple of Template:Math; this condition (see Bragg condition section below) was first presented by Lawrence Bragg on 11 November 1912 to the Cambridge Philosophical Society.<ref>There are some sources, like the Academic American Encyclopedia, that attribute the discovery of the law to both W.L Bragg and his father W.H. Bragg, but the official Nobel Prize site and the biographies written about him ("Light Is a Messenger: The Life and Science of William Lawrence Bragg", Graeme K. Hunter, 2004 and "Great Solid State Physicists of the 20th Century", Julio Antonio Gonzalo, Carmen Aragó López) make a clear statement that Lawrence Bragg alone derived the law.</ref> Although simple, Bragg's law confirmed the existence of real particles at the atomic scale, as well as providing a powerful new tool for studying crystals. Lawrence Bragg and his father, William Henry Bragg, were awarded the Nobel Prize in physics in 1915 for their work in determining crystal structures beginning with NaCl, ZnS, and diamond.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> They are the only father-son team to jointly win.

The concept of Bragg diffraction applies equally to neutron diffraction<ref>Template:Cite journal</ref> and approximately to electron diffraction.<ref name=":0">John M. Cowley (1975) Diffraction physics (North-Holland, Amsterdam) Template:ISBN.</ref> In both cases the wavelengths are comparable with inter-atomic distances (~ 150 pm). Many other types of matter waves have also been shown to diffract,<ref>Template:Cite journal</ref><ref>Template:Cite journal</ref> and also light from objects with a larger ordered structure such as opals.<ref name="Pieranski_1983" />

Bragg conditionEdit

File:Bragg diffraction 2.svg
Bragg diffraction<ref name="bragg">Template:Cite book</ref>Template:Rp Two beams with identical wavelength and phase approach a crystalline solid and are scattered off two different atoms within it. The lower beam traverses an extra length of 2dsinθ. Constructive interference occurs when this length is equal to an integer multiple of the wavelength of the radiation.

Bragg diffraction occurs when radiation of a wavelength Template:Mvar comparable to atomic spacings is scattered in a specular fashion (mirror-like reflection) by planes of atoms in a crystalline material, and undergoes constructive interference.<ref name="moseley1913a"/> When the scattered waves are incident at a specific angle, they remain in phase and constructively interfere. The glancing angle Template:Mvar (see figure on the right, and note that this differs from the convention in Snell's law where Template:Mvar is measured from the surface normal), the wavelength Template:Mvar, and the "grating constant" Template:Mvar of the crystal are connected by the relation:<ref name="Mose1913" />Template:Rp<math display="block">n\lambda = 2 d\sin\theta</math>where <math> n </math> is the diffraction order (<math> n = 1 </math> is first order, <math> n = 2 </math> is second order,<ref name="moseley1913a">Template:Cite journal</ref>Template:Rp <math> n = 3 </math> is third order<ref name="Mose1913">Template:Cite journal</ref>Template:Rp). This equation, Bragg's law, describes the condition on θ for constructive interference.<ref>Template:Cite book</ref>

A map of the intensities of the scattered waves as a function of their angle is called a diffraction pattern. Strong intensities known as Bragg peaks are obtained in the diffraction pattern when the scattering angles satisfy Bragg condition. This is a special case of the more general Laue equations, and the Laue equations can be shown to reduce to the Bragg condition with additional assumptions.<ref name=":1">Template:Cite book</ref>

DerivationEdit

In Bragg's original paper he describes his approach as a Huygens' construction for a reflected wave.<ref name="Bragg-1914">Template:Cite journal</ref>Template:Rp Suppose that a plane wave (of any type) is incident on planes of lattice points, with separation <math>d</math>, at an angle <math>\theta</math> as shown in the Figure. Points A and C are on one plane, and B is on the plane below. Points ABCC' form a quadrilateral.<ref>Template:Cite book</ref>Template:Rp

There will be a path difference between the ray that gets reflected along AC' and the ray that gets transmitted along AB, then reflected along BC. This path difference is <math display="block">(AB + BC) - \left(AC'\right) \,.</math>

The two separate waves will arrive at a point (infinitely far from these lattice planes) with the same phase, and hence undergo constructive interference, if and only if this path difference is equal to any integer value of the wavelength, i.e. <math display="block"> n\lambda =(AB + BC) - \left(AC'\right) </math>

where <math>n</math> and <math>\lambda</math> are an integer and the wavelength of the incident wave respectively.

Therefore, from the geometry <math display="block">AB = BC = \frac{d}{\sin\theta} \text{ and } AC = \frac{2d}{\tan\theta} \,,</math>

from which it follows that <math display="block">AC' = AC\cdot\cos\theta = \frac{2d}{\tan\theta}\cos\theta = \left(\frac{2d}{\sin\theta}\cos\theta\right)\cos\theta = \frac{2d}{\sin\theta}\cos^2\theta \,.</math>

Putting everything together, <math display="block">n\lambda = \frac{2d}{\sin\theta} - \frac{2d}{\sin\theta}\cos^2\theta = \frac{2d}{\sin\theta}\left(1 - \cos^2\theta\right) = \frac{2d}{\sin\theta}\sin^2\theta</math>

which simplifies to <math>n\lambda = 2d\sin\theta \,,</math> which is Bragg's law shown above.

If only two planes of atoms were diffracting, as shown in the Figure then the transition from constructive to destructive interference would be gradual as a function of angle, with gentle maxima at the Bragg angles. However, since many atomic planes are participating in most real materials, sharp peaks are typical.<ref name=":0" /><ref name=":1" />

A rigorous derivation from the more general Laue equations is available (see page: Laue equations).

Beyond Bragg's lawEdit

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File:DifraccionElectronesMET.jpg
Typical selected area electron diffraction pattern. Each spot corresponds to a different diffracted direction.

The Bragg condition is correct for very large crystals. Because the scattering of X-rays and neutrons is relatively weak, in many cases quite large crystals with sizes of 100 nm or more are used. While there can be additional effects due to crystal defects, these are often quite small. In contrast, electrons interact thousands of times more strongly with solids than X-rays,<ref name=":0" /> and also lose energy (inelastic scattering).<ref>Template:Cite journal</ref> Therefore samples used in transmission electron diffraction are much thinner. Typical diffraction patterns, for instance the Figure, show spots for different directions (plane waves) of the electrons leaving a crystal. The angles that Bragg's law predicts are still approximately right, but in general there is a lattice of spots which are close to projections of the reciprocal lattice that is at right angles to the direction of the electron beam. (In contrast, Bragg's law predicts that only one or perhaps two would be present, not simultaneously tens to hundreds.) With low-energy electron diffraction where the electron energies are typically 30-1000 electron volts, the result is similar with the electrons reflected back from a surface.<ref>Template:Cite book</ref> Also similar is reflection high-energy electron diffraction which typically leads to rings of diffraction spots.<ref>Template:Cite book</ref>

With X-rays the effect of having small crystals is described by the Scherrer equation.<ref name=":1" /><ref>Template:Cite journal</ref><ref>Template:Cite journal</ref> This leads to broadening of the Bragg peaks which can be used to estimate the size of the crystals.

Bragg scattering of visible light by colloidsEdit

A colloidal crystal is a highly ordered array of particles that forms over a long range (from a few millimeters to one centimeter in length); colloidal crystals have appearance and properties roughly analogous to their atomic or molecular counterparts.<ref name='Pieranski_1983'>Template:Cite journal</ref> It has been known for many years that, due to repulsive Coulombic interactions, electrically charged macromolecules in an aqueous environment can exhibit long-range crystal-like correlations, with interparticle separation distances often being considerably greater than the individual particle diameter. Periodic arrays of spherical particles give rise to interstitial voids (the spaces between the particles), which act as a natural diffraction grating for visible light waves, when the interstitial spacing is of the same order of magnitude as the incident lightwave.<ref name='Hiltner_1969'>Template:Cite journal</ref><ref name='Aksay_1984'>Template:Cite journal</ref><ref name="LuckKlier1963">Template:Cite journal</ref> In these cases brilliant iridescence (or play of colours) is attributed to the diffraction and constructive interference of visible lightwaves according to Bragg's law, in a matter analogous to the scattering of X-rays in crystalline solid. The effects occur at visible wavelengths because the interplanar spacing Template:Mvar is much larger than for true crystals. Precious opal is one example of a colloidal crystal with optical effects.

Volume Bragg gratingsEdit

{{#invoke:Labelled list hatnote|labelledList|Main article|Main articles|Main page|Main pages}} Volume Bragg gratings (VBG) or volume holographic gratings (VHG) consist of a volume where there is a periodic change in the refractive index. Depending on the orientation of the refractive index modulation, VBG can be used either to transmit or reflect a small bandwidth of wavelengths.<ref>Template:Cite journal</ref> Bragg's law (adapted for volume hologram) dictates which wavelength will be diffracted:<ref name=":2">Template:Cite book</ref>

<math display="block">2\Lambda\sin(\theta + \varphi)=m\lambda_B \,,</math>

where Template:Mvar is the Bragg order (a positive integer), Template:Math the diffracted wavelength, Λ the fringe spacing of the grating, Template:Mvar the angle between the incident beam and the normal (Template:Math) of the entrance surface and Template:Mvar the angle between the normal and the grating vector (Template:Math). Radiation that does not match Bragg's law will pass through the VBG undiffracted. The output wavelength can be tuned over a few hundred nanometers by changing the incident angle (Template:Mvar). VBG are being used to produce widely tunable laser source or perform global hyperspectral imagery (see Photon etc.).<ref name=":2" />

Selection rules and practical crystallographyEdit

{{#invoke:Labelled list hatnote|labelledList|Main article|Main articles|Main page|Main pages}} The measurement of the angles can be used to determine crystal structure, see x-ray crystallography for more details.<ref name=":0" /><ref name=":1" /> As a simple example, Bragg's law, as stated above, can be used to obtain the lattice spacing of a particular cubic system through the following relation:

<math display="block">d = \frac{a}{\sqrt{h^2 + k^2 + \ell^2}} \,,</math>

where <math>a</math> is the lattice spacing of the cubic crystal, and Template:Mvar, Template:Mvar, and Template:Mvar are the Miller indices of the Bragg plane. Combining this relation with Bragg's law gives:

<math display="block">\left(\frac{\lambda}{2a}\right)^2 = \left(\frac{\lambda}{2d}\right)^2 \frac{1}{h^2 + k^2 + \ell^2}</math>

One can derive selection rules for the Miller indices for different cubic Bravais lattices as well as many others, a few of the selection rules are given in the table below.

Selection rules for the Miller indices
Bravais lattices Example compounds Allowed reflections Forbidden reflections
Simple cubic Po Any h, k, None
Body-centered cubic Fe, W, Ta, Cr h + k + = even h + k + = odd
Face-centered cubic (FCC) Cu, Al, Ni, NaCl, LiH, PbS h, k, all odd or all even h, k, mixed odd and even
Diamond FCC Si, Ge All odd, or all even with h + k + = 4n h, k, mixed odd and even, or all even with h + k + ≠ 4n
Triangular lattice Ti, Zr, Cd, Be even, h + 2k ≠ 3n h + 2k = 3n for odd

These selection rules can be used for any crystal with the given crystal structure. KCl has a face-centered cubic Bravais lattice. However, the K+ and the Cl ion have the same number of electrons and are quite close in size, so that the diffraction pattern becomes essentially the same as for a simple cubic structure with half the lattice parameter. Selection rules for other structures can be referenced elsewhere, or derived. Lattice spacing for the other crystal systems can be found here.

See alsoEdit

ReferencesEdit

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Further readingEdit

  • Neil W. Ashcroft and N. David Mermin, Solid State Physics (Harcourt: Orlando, 1976).
  • Template:Cite journal

External linksEdit

Template:Crystallography