X-ray Diffraction (XRD)

• 1.0 What is X-ray Diffraction

• 2.0 Basics of Crystallography
• 3.0 Production of X-rays
• 4.0 Applications of XRD
• 5.0 Instrumental Sources of Error
• 6.0 Conclusions
 Bragg’s Law

n λ =2dsinθ

English physicists Sir W.H. Bragg and his son Sir W.L. Bragg
developed a relationship in 1913 to explain why the cleavage
faces of crystals appear to reflect X-ray beams at certain angles of
incidence (theta, θ). The variable d is the distance between atomic
layers in a crystal, and the variable lambda λ is the wavelength of
the incident X-ray beam; n is an integer. This observation is an
example of X-ray wave interference
(Roentgenstrahlinterferenzen), commonly known as X-ray
diffraction (XRD), and was direct evidence for the periodic atomic
structure of crystals postulated for several centuries.
 Bragg’s Law

n λ =2dsinθ

The Braggs were awarded the Nobel Prize in

physics in 1915 for their work in determining
crystal structures beginning with NaCl, ZnS
and diamond.

Although Bragg's law was used to explain the interference pattern

of X-rays scattered by crystals, diffraction has been developed to
study the structure of all states of matter with any beam, e.g., ions,
electrons, neutrons, and protons, with a wavelength similar to the
distance between the atomic or molecular structures of interest.
 Deriving Bragg’s Law: nλ = 2dsinθ
X-ray 1
Constructive interference X-ray 2
occurs only when

n λ = AB + BC AB+BC = multiples of nλ

AB=BC

n λ = 2AB

Sinθ=AB/d

AB=dsinθ

n λ =2dsinθ

λ = 2dhklsinθhkl
 Constructive and Destructive
Interference of Waves

Constructive Interference Destructive Interference

In Phase Out of Phase
 1.0 What is X-ray Diffraction ?
I

www.micro.magnet.fsu.edu/primer/java/interference/index.html
 Why XRD?

• Measure the average spacings between

layers or rows of atoms
• Determine the orientation of a single
crystal or grain
• Find the crystal structure of an unknown
material
• Measure the size, shape and internal
stress of small crystalline regions
 X-ray Diffraction (XRD)
The atomic planes of a crystal cause an incident beam of X-rays to
interfere with one another as they leave the crystal. The phenomenon is
called X-ray diffraction.

Effect of sample
incident beam
thickness on the
absorption of X-rays

crystal diffracted beam

film

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 Detection of Diffracted X-rays
by Photographic film
sample
film

X-ray
Point where Film
incident beam
enters
2θ = 0°
2θ = 180°

Debye - Scherrer Camera

A sample of some hundreds of crystals (i.e. a powdered sample) show that the diffracted
beams form continuous cones. A circle of film is used to record the diffraction pattern as
shown. Each cone intersects the film giving diffraction lines. The lines are seen as arcs
on the film.
 Bragg’s Law and Diffraction:
How waves reveal the atomic structure of crystals
n λ = 2dsinθ n-integer
Diffraction occurs only when Bragg’s Law is satisfied Condition for constructive
interference (X-rays 1 & 2) from planes with spacing d

X-ray1

X-ray2
l
λ=3Å
θ=30o
Atomic
plane
d=3 Å

2θ-diffraction angle

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 Planes in Crystals-2 dimension
λ = 2dhklsinθhkl

Different planes
have different
spacings

To satisfy Bragg’s Law, θ must change as d changes

e.g., θ decreases as d increases.
 2.0 Basics of Crystallography
smallest building block
c
d3
βα
b
a γ
Unit cell
(Å)
d1
Beryl crystals CsCl
(cm) Lattice d2
A crystal consists of a periodic arrangement of the unit cell into a
lattice. The unit cell can contain a single atom or atoms in a fixed
arrangement.
Crystals consist of planes of atoms that are spaced a distance d apart,
but can be resolved into many atomic planes, each with a different d-
spacing.
a,b and c (length) and α, β and γ angles between a,b and c are lattice
constants or parameters which can be determined by XRD.
Seven Crystal Systems - Review
 Miller Indices: hkl - Review

Miller indices-the reciprocals of the

fractional intercepts which the plane
makes with crystallographic axes

(010)

a b c a b c
Axial length 4Å 8Å 3Å 4Å 8Å 3Å
Intercept lengths 1Å 4Å 3Å ∞ 8Å ∞
Fractional intercepts ¼ ½ 1 0 1 0
Miller indices 4 2 1 0 1 0
h k l h k l
4/ ∞ =0
Several Atomic Planes and Their d-spacings in
a Simple Cubic - Review

a b c a b c
1 0 0 1 1 0
1 0 0 1 1 0

d100
Cubic
(100) a=b=c=a0
(110)

a b c
a b c
d012 0 1½
1 1 1
0 1 2
1 1 1

(111) (012)
Black numbers-fractional intercepts, Blue numbers-Miller indices
Planes and Spacings - Review
 Indexing of Planes and Directions -
Review

(111)
c c

b b
a a [110]

a direction: [uvw] a plane: (hkl)

<uvw>: a set of equivalent {hkl}: a set of equi-
directions valent planes
 3.0 Production of X-rays

Cross section of sealed-off filament X-ray tube

copper vacuum glass
X-rays
tungsten filament

electrons
cooling
water
to transformer
target
Vacuum

beryllium window X-rays metal focusing cap

X-rays are produced whenever high-speed electrons collide with a metal

target. A source of electrons – hot W filament, a high accelerating voltage
between the cathode (W) and the anode and a metal target, Cu, Al, Mo,
Mg. The anode is a water-cooled block of Cu containing desired target
metal.
 Characteristic X-ray Lines
Kα
Kβ and Kα2 will cause
extra peaks in XRD pattern,
and shape changes, but
can be eliminated by
Kα1
adding filters.
Intensity

<0.001Å
----- is the mass
absorption coefficient of
Kα2
Zr.
Kβ

λ (Å)
Spectrum of Mo at 35kV
 Specimen Preparation

Powders: 0.1µm < particle size <40 µm

Peak broadening less diffraction occurring
Double sided tape

Glass slide

Bulks: smooth surface after polishing, specimens should be

thermal annealed to eliminate any surface deformation
induced during polishing.
 JCPDS Card Quality of data

1.file number 2.three strongest lines 3.lowest-angle line 4.chemical

formula and name 5.data on diffraction method used 6.crystallographic
data 7.optical and other data 8.data on specimen 9.data on diffraction pattern.
Joint Committee on Powder Diffraction Standards, JCPDS (1969)
Replaced by International Centre for Diffraction Data, ICDF (1978)
A Modern Automated X-ray Diffractometer

Detector
X-ray Tube
2θ
θ

Sample stage

Cost: $560K to 1.6M

Basic Features of Typical XRD Experiment

1) Production
X-ray tube
2) Diffraction

3) Detection

4) Interpretation
Detection of Diffracted X-rays
by a Diffractometer

C
Circle of Diffractometer

Recording

Amplifier
Focalization
Circle

Detector
Photon counter

Bragg - Brentano Focus Geometry, Cullity

 Peak Position
d-spacings and lattice parameters

λ = 2dhklsinθhkl
Fix λ (Cu kα) = 1.54Å dhkl = 1.54Å/2sinθhkl
(Most accurate d-spacings are those calculated from high-angle peaks)

For a simple cubic (a = b = c = a 0)

a0
d hkl =
h +k +l
2 2 2

a0 = dhkl /(h2+k2+l2)½
e.g., for NaCl, 2θ220=46o, θ220=23o,
d220 =1.9707Å, a0=5.5739Å
 Bragg’s Law and Diffraction:
How waves reveal the atomic structure of crystals
n λ = 2dsinθ n-integer
Diffraction occurs only when Bragg’s Law is satisfied Condition for constructive
interference (X-rays 1 & 2) from planes with spacing d

X-ray1

a0 = dhkl /(h2+k2+l2X-ray2
)½ l
220=46 , θ220=23 ,
e.g., for NaCl, 2θλ=3Å o o
θ=30o
d220 =1.9707Å, a0=5.5739Å Atomic
plane
d=3 Å

2θ-diffraction angle

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 XRD Pattern of NaCl Powder

(Cu Kα)

Miller indices: The peak is due to X-

ray diffraction from the {220}
planes.

Diffraction angle 2θ (degrees)

Significance of Peak Shape in XRD

1. Peak position
2. Peak width
3. Peak intensity
 Peak Width-Full Width at Half Maximum

FWHM Important for:

Peak position 2θ • Particle or
grain size
mode 2. Residual
Imax
max strain

Can also be fit with Gaussian,

Lerentzian, Gaussian-Lerentzian etc.
Intensity

I max
2
Background

Bragg angle 2θ
Effect of Lattice Strain on Diffraction
Peak Position and Width
Diffraction
Line

do
No Strain

Uniform Strain d1
(d1-do)/do
Peak moves, no shape changes
Shifts to lower angles

Non-uniform Strain
d1≠constant
RMS Strain
Peak broadens
Exceeds d0 on top, smaller than d0 on the bottom
 4.0 Applications of XRD

• XRD is a nondestructive technique

• To identify crystalline phases and orientation
• To determine structural properties:
Lattice parameters (10-4Å), strain, grain size,
expitaxy, phase composition, preferred orientation
(Laue) order-disorder transformation, thermal
expansion
• To measure thickness of thin films and multi-layers*
• To determine atomic arrangement
• Detection limits: ~3% in a two phase mixture; can be
~0.1% with synchrotron radiation
Spatial resolution: normally none
 Phase Identification

One of the most important uses of XRD!!!

• Obtain XRD pattern
• Measure d-spacings
• Obtain integrated intensities
• Compare data with known standards in the
JCPDS file, which are for random orientations
(there are more than 50,000 JCPDS cards of
inorganic materials).
 Mr. Hanawalt
Powder diffraction files: The task of building up a collection of known
patterns was initiated by Hanawalt, Rinn, and Fevel at the Dow Chemical
Company (1930’s). They obtained and classified diffraction data on
some 1000 substances. After this point several societies like ASTM
(1941-1969) and the JCPS began to take part (1969-1978). In 1978 it was
renamed the Int. Center for Diffraction Data (ICDD) with 300 scientists
worldwide. In 1995 the powder diffraction file (PDF) contained nearly
62,000 different diffraction patterns with 200 new being added each
year. Elements, alloys, inorganic compounds, minerals, organic
compounds, organo-metallic compounds.

Hanawalt: Hanawalt decided that since more than one substance can
have the same or nearly the same d value, each substance should be
characterized by it’s three strongest lines (d1, d2, d3). The values of d1-
d3 are usually sufficient to characterize the pattern of an unknown and
enable the corresponding pattern in the file to be located.
 Phase Identification
a b c - Effect of Symmetry
on XRD Pattern
a. Cubic
a=b=c, (a)

b. Tetragonal
2θ a=b≠c (a and c)

c. Orthorhombic
a≠b≠c (a, b and c)

• Number of reflections
• Peak position
• Peak splitting
 More Applications of XRD

a Diffraction patterns of three

(004) Superconducting thin films
annealed for different times.

a. Tl2CaBa2Cu2Ox (2122)
b b. Tl2CaBa2Cu2Ox (2122) +
Intensity

Tl2Ca2Ba2Cu3Oy (2223)
b=a+c
c. Tl2Ca2Ba2Cu3Oy (2223)
c
(004) CuO was detected by
comparison to standards
 XRD Studies

• Temperature

• Electric Field

• Pressure

• Deformation
 Effect of Coherent Domain Size
As rolled As rolled 300oC

HARDNESS (Rockwell B)
Increasing Grain size (t)
200oC

Kα1
Kα2
Intensity

250oC 450oC

300oC ANNEALING TEMPERATURE (°C)

0.9 ⋅ λ
B= Peak Broadening
450oC t ⋅ Cosθ Scherrer Model

As grain size decreases hardness

2θ
(331) Peak of cold-rolled and
increases and peaks become
Annealed 70Cu-30Zn (brass) broader
High Temperature XRD Patterns of the
Decomposition of YBa2Cu3O7-δ

I
Intensity (cps)

2θ
 In Situ X-ray Diffraction Study of an Electric Field
Induced Phase Transition

(330) Single Crystal Ferroelectric

92%Pb(Zn 1/3Nb2/3)O3 -8%PbTiO3
Intensity (cps) Intensity (cps)

E=6kV/cm (330) peak splitting is due to

Presence of <111> domains
Kα1
Rhombohedral phase
Kα2

E=10kV/cm No (330) peak splitting

Kα1 Tetragonal phase

Kα2
 What Is A Synchrotron?
A synchrotron is a particle acceleration device which,
through the use of bending magnets, causes a charged
particle beam to travel in a circular pattern.
Advantages of using synchrotron radiation:
•Detecting the presence and quantity of trace elements
•Providing images that show the structure of materials
•Producing X-rays with 108 more brightness than those from
normal X-ray tube (tiny area of sample)
•Having the right energies to interact with elements in light
atoms such as carbon and oxygen
•Producing X-rays with wavelengths (tunable) about the size
of atom, molecule and chemical bonds
 Synchrotron Light Source
Diameter: 2/3 length of a football field

Cost: $Bi
5.0 Instrumental Sources of Error

• Specimen displacement
• Instrument misalignment
• Error in zero 2θ position
• Peak distortion due to Kα2 and Kβ wavelengths
 6.0 Conclusions

• Non-destructive, fast, easy sample prep

• High-accuracy for d-spacing calculations

• Can be done in-situ

• Single crystal, poly, and amorphous materials

• Standards are available for thousands of material

systems
 XRF: X-Ray Fluorescence

XRF is a ND technique used for chemical analysis of materials. An X-

ray source is used to irradiate the specimen and to cause the elements
in the specimen to emit (or fluoresce) their characteristic X-rays. A
detection system (wavelength dispersive) is used to measure the
peaks of the emitted X-rays for qual/quant measurements of the
elements and their amounts. The techniques was extended in the
1970’s to to analyze thin films. XRF is routinely used for the
simultaneous determination of elemental composition and film
thickness.
Analyzing Crystals used: LiF (200), (220), graphite (002), W/Si, W/C,
V/C, Ni/C
1) X-ray irradiates specimen XRF Setup
2) Specimen emits characteristic
X-rays or XRF
3) Analyzing crystal rotates to NiKα
accurately reflect each I
wavelength and satisfy 4)
Bragg’s Law
4) Detector measures position 2φ
and intensity of XRF peaks

1)

2) 3)
XRF is diffracted by a
crystal at different φ to
nλ=2dsinφ - Bragg’s Law separate X-ray λ and to
identify elements
 Preferred Orientation
A condition in which the distribution of crystal orientations is
non-random, a real problem with powder samples.

Random orientation ------

Intensity Preferred orientation ------

It is noted that due to preferred orientation several blue peaks are

completely missing and the intensity of other blue peaks is very misleading.
Preferred orientation can substantially alter the appearance of the powder
pattern. It is a serious problem in experimental powder diffraction.
 3. By Laue Method - 1st Method Ever Used
Today - To Determine the Orientation of Single Crystals

Back-reflection Laue

crystal
[001]
X-ray Film

pattern

Transmission Laue
crystal
Film