Crystal Structure and Defects

– Microstructure
– Crystal Structure and Crystallography
– Crystal Defects
 Microstructure of Materials
¾ Spatial arrangements of atoms play an important role in
determining the electrical properties.
¾ Solids are classified into three broad classifications:
¾ Amorphous: no recognizable long range order
¾ Crystalline: Entire solid is made up of atoms in an orderly array
¾ Polycrystalline: Completely ordered in segments

Amorphous Polycrystalline Crystalline

 Microstructure of Materials

Amorphous Polycrystalline Crystalline

 Crystal Structure
¾ Crystal structures are regular 3-dimensional patterns of atoms in space
¾ The regularity with which atoms are packed in solids arises from geometrical
conditions (i.e., bond angles and lengths) which are imposed by directional
bonding and close packing
¾ Most stable arrangement will be the one that
1) Minimizes energy/volume
2) Preserves electrical neutrality
3) Satisfies directionality and discreteness of the covalent bonds
4) Minimizes ion-ion repulsion
5) Packs atoms as closely as possible consistent with (1)-(5)
 Description of Crystal Structure: Lattice
¾ A lattice is an infinite three dimensional array of points in
which every point has surroundings identical with that of
every other point. These are called lattice points.

¾ Example: A 2-D square space lattice:

r
Set of all points r ' defined by
r r r r r
r'= r + u a + u a + u a
1 1 2 2 3 3

where u1, u2, u3 are integers

a1
a2
 Bravais Space Lattices
¾ The most general (“lowest symmetry”) 2-D lattice is the “oblique lattice”
in 2-D.
¾ a1 and a2 are called lattice translation vectors. Translation by integer
multiple of a1 and a2 takes one from one lattice point to another
¾ There is an infinite number of lattices because there are no restrictions on
the length or the angle (α) between the lattice translation vectors.
¾ But restrictions on the number of lattices are placed if relations between
lengths of a1 and a2 and α are specified

2-D Oblique lattice a1

α
a2
 Bravais Lattices in 2-D
¾ 4 restrictions that can be imposed on a1,a2 and α gives rise to
total of 5 Bravais lattices in 2-D (1 general, 4 special lattices).
 14 Bravais Space Lattices in 3-D

http://www.chem.ox.ac.uk/icl/heyes/structure_of_solids/Lecture1/Bravais.gif
 Specifying Crystal Structure
¾ A motif or a basis is a specific arrangement of atoms which
belong to a lattice point.
¾ Crystal structure can be completely described by specification
of a lattice and basis

Lattice + Basis = Crystal Structure

a
a

Lattice is square lattice

Basis is large red atom at (0,0) and small blue atom at (½ a, ½ a)
 Unit Cell
¾ Moving the basis from lattice point to lattice point
generates a crystal structure.
¾ A unit cell is a repeating unit of the space lattice which can
be used to reproduce the entire cell. Lattice + basis
specifies a unit cell.
¾ Primitive unit cell is one that has only one atom per unit
cell and the lattice vectors defining the cell are said to be
primitive lattice vectors.
¾ We often use primitive translation vectors and unit cells to
define the crystal structure but nonprimitive axes are also
used when they have simpler relation to the symmetry of
the structure.
 Simple 3-D Unit Cells: Simple cubic (SC)

¾ 1 lattice points per cell

¾ Po crystal structure = SC lattice + 1 atom at lattice sites
¾ 6 nearest neighbors at a (a = lattice parameter)
Simple 3-D Unit Cells: Body centered cubic (BCC)

¾ 2 lattice points per cell

¾ Mo, W crystal structure = BCC lattice + 1 atom at lattice sites
¾ 8 nearest neighbors at 0.87 a
BCC Primitive Unit Cell
FCC Unit Cell and FCC Crystal Structure

¾ 4 lattice points per cell

¾ Cu, Au, Ag, Pt, etc.
crystal structure =
FCC lattice + 1 atom at
lattice sites
¾ 12 nearest neighbors;
close packed structure
FCC Primitive Unit Cell
 The Diamond Lattice
¾ The crystal structure of group IV semiconductors (Si and Ge) is
described by unit cell known as the diamond lattice unit cell
¾ Diamond structure is an FCC Bravais lattice with a basis that has two
identical (e.g., Si, Ge, or C) atoms at each and of the vector
(¼,¼,¼)a, where a is the lattice constant (different for Si, Ge and C).
Diamond Structure
 The Diamond Lattice
¾ A less formal way of visualizing the diamond structure is to think of
it in terms of two FCC lattices interpenetrating each other.
¾ One FCC lattice is shifted with respect to the other along the body
diagonal by ¼ of the body diagonal length
 The Zincblende Structure
¾ GaAs has the Zinc blende structure
¾ An FCC Bravais lattice with a basis that has two different atoms one
at the each end of the vector (¼,¼,¼)a (e.g., Ga on one end and As on
the other end)
¾ Zincblende structure is the same as the diamond structure (two FCC
lattices interpenetrating each other with one FCC lattice shifted with
respect to the other along the body diagonal by ¼ of the body
diagonal length) but the two FCC lattices are made of different atoms
The Zincblende Structure
 Miller Indices
¾ Miller indices help specify atomic planes and orientations in a crystal
¾ To obtain Miller indices of any plane of atoms do the following.
1) Set up coordinate axes along the edges of the unit cell and note
where the plane in question intercepts the axes (x,y,z).
2) Take the reciprocal of the intercepts.
3) Using appropriate multiplier convert the reciprocals obtained to
smallest set of whole numbers.
4) By convention these numbers (h,k,l) are enclosed in () to identify
a plane. If any of the numbers have a negative sign a bar is
located at the top of that index.
¾ Equivalent planes (family of planes that contain identical atomic
arrangements) are referenced by enclosing one of the members of the
group in {}. e.g., in diamond structure
{001}=(100), (010), (001), ( 1 00), (0 1 0), (00 1 )
 Miller Indices Examples

¾ Plane intercepts x,y,z axes at 3a1, 2a2, and 2a3 repectively

¾ Reciprocals are 1/3, 1/2, and 1/2
¾ To get smallest integers having this ratio multiply by common
denominator 6. Thus this is the (233) plane
Miller Indices Examples
 Crystallographic Directions

¾ Miller indices enclosed within [ ] are used to designate

directions within a crystal
¾ Note also that the Miller indices also give the direction of
the normal vector of the plane they describe
¾ Miller indices enclosed within < > are used to designate
equivalent (family of) directions.
e.g., in simple cubic lattice [100] is the x-axis direction,
<100> describes all directions parallel to the x, y and z
axis.
 Crystal Defects

¾ Defects are imperfections which cause disruption in

what otherwise would be a perfect lattice.
¾ Defects are classified based on their dimensionality
¾ Point defects (0-D)
¾ Line defects (1-D)
¾ Surface Imperfections (2-D)
¾ Volume defects (3-D)
 Point Defects
¾ Vacancy: absence of an atom in a lattice point where there is
suppose to be an atom. Formed when atoms are removed from
their lattice positions (typically to the surface) as a result of
thermal fluctuations. AKA Schottky defects.
¾ Interstitial: Atom located in a “void” (I.e., a position that is not
part of the lattice or basis) within the crystal structure.
¾ Frenkel Defect: A vacancy-interstitial pair.
¾ Substitutional Impurity: Impurity atoms (an atom that does not
belong to the basis) that take up the lattice positions that are
ordinarily occupied by the atoms that make up the crystal.
¾ Interstitial Impurity: Impurity atoms that are present in the
interstitial sites.
Point Defects
Point Defects
 Line Defects
¾ Dislocations: Boundary between two regions of a surface
which are perfect themselves but are out of registry with each
other. The resulting lattice distortion is centered along a line.
¾ Burgers Vector, b: A vector by which the lattice on one side
of an internal surface containing the dislocation line is
displace relative to the lattice on the other side.
¾ There are two special cases of dislocations
¾ Edge Dislocation: b and normal vector along the
dislocation line l are perpendicular
¾ Screw Dislocation: b and normal vector along the
dislocation line l are parallel
 Line Defects
Edge Dislocation Screw Dislocation