# Bragg's law

(Redirected from Bragg’s law)
"Bragg scattering" redirects here. For wind waves radar remote sensing, see Wave radar.

In physics, Bragg's law gives the angles for coherent and incoherent scattering from a crystal lattice. When X-rays are incident on an atom, they make the electronic cloud move as does any electromagnetic wave. The movement of these charges re-radiates waves with the same frequency (blurred slightly due to a variety of effects); this phenomenon is known as Rayleigh scattering (or elastic scattering). The scattered waves can themselves be scattered but this secondary scattering is assumed to be negligible.

A similar process occurs upon scattering neutron waves from the nuclei or by a coherent spin interaction with an unpaired electron. These re-emitted wave fields interfere with each other either constructively or destructively (overlapping waves either add together to produce stronger peaks or subtract from each other to some degree), producing a diffraction pattern on a detector or film. The resulting wave interference pattern is the basis of diffraction analysis. This analysis is called Bragg diffraction.

Bragg diffraction (also referred to as the Bragg formulation of X-ray diffraction) was first proposed by William Lawrence Bragg and William Henry Bragg in 1913 in response to their discovery that crystalline solids produced surprising patterns of reflected X-rays (in contrast to that of, say, a liquid). They found that these crystals, at certain specific wavelengths and incident angles, produced intense peaks of reflected radiation (known as Bragg peaks). The concept of Bragg diffraction applies equally to neutron diffraction and electron diffraction processes.[1] Both neutron and X-ray wavelengths are comparable with inter-atomic distances (~150 pm) and thus are an excellent probe for this length scale.

X-rays interact with the atoms in a crystal.

W. L. Bragg explained this result by modeling the crystal as a set of discrete parallel planes separated by a constant parameter d. It was proposed that the incident X-ray radiation would produce a Bragg peak if their reflections off the various planes interfered constructively. The interference is constructive when the phase shift is a multiple of $2\pi$; this condition can be expressed by Bragg's law:[2]

$n\lambda = 2d\sin\theta \,,$

where n is an integer, λ is the wavelength of incident wave, d is the spacing between the planes in the atomic lattice, and θ is the angle between the incident ray and the scattering planes. Note that moving particles, including electrons, protons and neutrons, have an associated De Broglie wavelength.

According to the 2θ deviation, the phase shift causes constructive (left figure) or destructive (right figure) interferences.

Bragg's Law was derived by physicist Sir William Lawrence Bragg[3] in 1912 and first presented on 11 November 1912 to the Cambridge Philosophical Society. 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 in the form of X-ray and neutron diffraction. William Lawrence Bragg and his father, Sir 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. They are the only father-son team to jointly win. W. L. Bragg was 25 years old, making him the youngest Nobel laureate.

## Bragg condition

Bragg diffraction. 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 electromagnetic radiation or subatomic particle waves with wavelength comparable to atomic spacings are incident upon a crystalline sample, are scattered in a specular fashion by the atoms in the system, and undergo constructive interference in accordance to Bragg's law. For a crystalline solid, the waves are scattered from lattice planes separated by the interplanar distance d. Where the scattered waves interfere constructively, they remain in phase since the path length of each wave is equal to an integer multiple of the wavelength. The path difference between two waves undergoing constructive interference is given by 2dsinθ, where θ is the scattering angle. This leads to Bragg's law, which describes the condition for constructive interference from successive crystallographic planes (h, k, and l, as given in Miller Notation)[4] of the crystalline lattice:

$2 d\sin\theta = n\lambda \,,$

where n is an integer determined by the order given, and λ is the wavelength.[5] A diffraction pattern is obtained by measuring the intensity of scattered waves as a function of scattering angle. Very strong intensities known as Bragg peaks are obtained in the diffraction pattern when scattered waves satisfy the Bragg condition.

It should be taken into account that if only two planes of atoms were diffracting, as shown in the pictures, then the transition from constructive to destructive interference would be gradual as the angle is varied. However, since many atomic planes are interfering in real materials, very sharp peaks surrounded by mostly destructive interference result.[6]

## Heuristic derivation

Suppose that a single monochromatic wave (of any type) is incident on aligned planes of lattice points, with separation $d$, at angle $\theta$. Points A and C are on one plane, and B is on the plane below. Points ABCC' form a quadrilateral.

There will be a path difference between the ray that gets reflected along AC' and the ray that gets transmitted, then reflected, along AB and BC respectively. This path difference is

$(AB+BC) - (AC') \,.$

The two separate waves will arrive at a point 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.

$(AB+BC) - (AC') = n\lambda \,,$

where the same definition of $n$ and $\lambda$ apply as above.

Therefore,

$AB = BC = \frac{d}{\sin\theta} \text{ and } AC = \frac{2d}{\tan\theta} \,,$

from which it follows that

$AC' = AC\cdot\cos\theta = \frac{2d}{\tan\theta}\cos\theta = \left(\frac{2d}{\sin\theta}\cos\theta\right)\cos\theta = \frac{2d}{\sin\theta}\cos^2\theta \,.$

Putting everything together,

$n\lambda = \frac{2d}{\sin\theta}(1-\cos^2\theta) = \frac{2d}{\sin\theta}\sin^2\theta \,,$

which simplifies to

$n\lambda = 2d\sin\theta \,,$

which is Bragg's law.

## Bragg scattering of visible light by colloids

A colloidal crystal is a highly ordered array of particles which can be formed over a very long range (from a few millimeters to one centimeter) in length, and which appear analogous to their atomic or molecular counterparts.[7] The periodic arrays of spherical particles make similar arrays of interstitial voids (the spaces between the particles), which act as a natural diffraction grating for visible light waves, especially when the interstitial spacing is of the same order of magnitude as the incident lightwave.[8][9][10]

Thus, 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. In all of these cases in nature, the same brilliant iridescence (or play of colours) can be attributed to the diffraction and constructive interference of visible lightwaves which satisfy Bragg’s law, in a matter analogous to the scattering of X-rays in crystalline solid.

## Selection rules and practical crystallography

Bragg's law, as stated above, can be used to obtain the lattice spacing of a particular cubic system through the following relation:

$d = \frac{a}{ \sqrt{h^2 + k^2 + l^2}} \,,$

where $a$ is the lattice spacing of the cubic crystal, and $h$, $k$, and $l$ are the Miller indices of the Bragg plane. Combining this relation with Bragg's law:

$\left( \frac{ \lambda\ }{ 2a } \right)^2 = \frac{ \sin ^2 \theta\ }{ h^2 + k^2 + l^2 } \,.$

One can derive selection rules for the Miller indices for different cubic Bravais lattices; here, selection rules for several will be given as is.

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

These selection rules can be used for any crystal with the given crystal structure. KCl exhibits a fcc cubic structure. 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.

## References

1. ^ John M. Cowley (1975) Diffraction physics (North-Holland, Amsterdam) ISBN 0-444-10791-6.
2. ^ See, for example, this example calculation of interatomic spacing with Bragg's law.
3. ^ 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 William Lawrence Bragg alone derived the law.
4. ^ H. P. Myers (2002). Introductory Solid State Physics. Taylor & Francis. ISBN 0-7484-0660-3.
5. ^ Carl. R. Nave. Bragg's Law. HyperPhysics, Georgia State University. Retrieved 2008-07-19.
6. ^
7. ^ Pieranski, P (1983). "Colloidal Crystals". Contemporary Physics 24: 25. Bibcode:1983ConPh..24...25P. doi:10.1080/00107518308227471.
8. ^ Hiltner, PA; IM Krieger (1969). "Diffraction of Light by Ordered Suspensions". Journal of Physical Chemistry 73: 2306. doi:10.1021/j100727a049.
9. ^ Aksay, IA (1984). "Microstructural Control through Colloidal Consolidation". Proceedings of the American Ceramic Society 9: 94.
10. ^ Luck, W. et al., Ber. Busenges Phys. Chem. , Vol. 67, p.84 (1963).