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CRYSTALLINE STATE

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Page 1: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

CRYSTALLINE STATE

Page 2: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

INTRODUCTIONElectro

nic structur

e

Bonding

State of aggrega

tion

Octet stability Primary:1. Ionic2. Covalent3. Metallic4. Van der Waals

Secondary:1. Dipole-dipole2. London dispersion3. Hydrogen

GasLiquidSolid

Page 3: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

STATE OF MATTER

GAS LIQUID SOLID

• The particles move rapidly

• Large space between particles

• The particles move past one another

• The particles close together

• Retains its volume

• The particles are arranged in tight and regular pattern

• The particles move very little

• Retains its shape and volume

Page 4: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

CLASSIFICATION OF SOLID BY ATOMIC ARRANGEMENT

Ordered

• regular• long-range• crystalline• “crystal”• transparent

Disordered

• random*• short-range*• amorphous• “glass”• opaque

Atomic arrangementOrderName

CRYSTAL SYSTEM

Page 5: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

EARLY CRYSTALLOGRAPHY

ROBERT HOOKE (1660) : canon ball

Crystal must owe its regular shape to the packing of spherical particles (balls) packed regularly, we get long-range order.

NEILS STEENSEN (1669) : quartz crystal

All crystals have the same angles between corresponding faces, regardless of their sizes he tried to make connection between macroscopic and atomic world.

If I have a regular cubic crystal, then if I divide it into smaller and smaller pieces down to an atomic dimension, will I get a cubic repeat unit?

Page 6: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

RENĖ-JUST HAŪY (1781): cleavage of calcite

• Common shape to all shards: rhombohedral

• Mathematically proved that there are only 7 distinct space-filling volume elements

7 CRYSTAL SYSTEMS

Page 7: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

CRYSTALLOGRAPHIC AXES

3 AXES 4 AXESyz = xz = xy =

yz = 90xy = yu = ux = 60

Page 8: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

THE SEVEN CRYSTAL SYSTEMS

Page 9: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London
Page 10: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

(rombhohedral)

Page 11: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

SPACE FILLING

TILING

Page 12: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London
Page 13: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London
Page 14: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London
Page 15: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London
Page 16: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London
Page 17: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

AUGUST BRAVAIS (1848): more math

How many different ways can we put atoms into these 7 crystal systems and get distinguishable point environment?

He mathematically proved that there are 14 distinct ways to arrange points in space

14 BRAVAIS LATTICES

Page 18: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

The Fourteen Bravais Lattices

Page 19: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

Simple cubic Body-centeredcubic

Face-centeredcubic

1 32

Page 20: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

4

Simple tetragonal Body-centered tetragonal

5

Page 21: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

Simple orthorhombic Body-centered orthorhombic

6 7

Page 22: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

8 9

Page 23: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

10 1211

Page 24: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

1413

Hexagonal

Page 25: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

A point lattice

Repeat unit

Page 26: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

z

x

y

A unit cell

O

b

a

c

a, b, c

, , Lattice parameters

Page 27: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

CRYSTAL STRUCTURE(Atomic arrangement in 3 space)

BRAVAIS LATTICE(Point environment)

BASIS(Atomic grouping at each lattice point)

Page 28: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

EXAMPLE: properties of cubic system*)

BRAVAIS LATTICE

BASIS CRYSTAL STRUCTURE

EXAMPLE

FCC atom FCC Au, Al, Cu, Pt

molecule FCC CH4

ion pair(Na+ and Cl -)

Rock salt NaCl

Atom pair DC (diamond crystal)

Diamond, Si, Ge

C

C109

*) cubic system is the most simplemost of elements in periodic table have cubic crystal structure

Page 29: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

CRYSTAL STRUCTURE OF NaCl

Page 30: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

CHARACTERISTIC OF CUBIC LATTICES

SC BCC FCCUnit cell volume a3 a3 a3

Lattice point per cell 1 2 4Nearest neighbor distance a a3 / 2 a/2Number of nearest neighbors (coordination no.)

6 8 12

Second nearest neighbor distance

a2 a a

Number of second neighbor 12 6 6a = f(r) 2r 4/3 r 22 r

or 4r = a4 a3 a2Packing density 0.52 0.68 0.74

Page 31: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

volumetotalatomsofvolume

densitypacking

3

3

344

a

r

EXAMPLE: FCC

3

3

223

44

r

r

74.02322

344

3

3

r

r

FCC74% matter (hard sphere model)

26% void

Page 32: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

• In crystal structure, atom touch in one certain direction and far apart along other direction.

• There is correlation between atomic contact and bonding.

• Bonding is related to the whole properties, e.g. mechanical strength, electrical property, and optical property.

• If I look down on atom direction: high density of atoms direction of strength; low density/population of atom direction of weakness.

• If I want to cleave a crystal, I have to understand crystallography.

Page 33: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London
Page 34: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

CRYSTALLOGRAPHIC NOTATION

POSITION: x, y, z, coordinate, separated by commas, no enclosure

O: 0,0,0

A: 0,1,1

B: 1,0,½

B

A

z

x

y

Unit cell

O

a

Page 35: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

DIRECTION: move coordinate axes so that the line passes through origin

Define vector from O to point on the line Choose the smallest set of integers No commas, enclose in brackets, clear fractions

OB 1 0 ½ [2 0 1]

AO 0 -1 -1 110

B

A

z

x

y

Unit cell

O

Page 36: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

Denote entire family of directions by carats < >

e.g.

all body diagonals: <1 1 1>

111 111 111 111

111 111 111 111

Page 37: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

all face diagonals: <0 1 1>

110 110 110

101

110

101 101 101

011 011 011 011

all cube edges: <0 0 1>

100 100 010 001 010 001

Page 38: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

MILLER INDICESFor describing planes.

Equation for plane: 1cz

by

ax

where a, b, and c are the intercepts of the plane with the x, y, and z axes, respectively.

Let:

so that

No commas, enclose in parenthesis (h k l) denote entirely family of planes by brace, e.g. all faces of unit

cell: {0 0 1}

ah

1

cl

1

bk

1

1 lzkyhx

100 100 001 etc.

Page 39: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

MILLER INDICES

a

b

cIntercept at

Intercept at a/2

Intercept at b

Miller indices: (h k l)

121

(2 1 0)

Parallel to z axes

(h k l) [h k l]

[2 1 0]

(2 1 0)

Page 40: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

Miller indices of planes in the cubic system

(0 1 0) (0 2 0)

011 111 210

011

Page 41: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

Many of the geometric shapes that appear in the crystalline state are some degree symmetrical.

This fact can be used as a means of crystal classification.

The three elements of symmetry:

Symmetry about a point (a center of symmetry)

Symmetry about a line (an axis of symmetry)

Symmetry about a plane (a plane of symmetry)

CRYSTAL SYMMETRY

Page 42: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

SYMMETRY ABOUT A POINT

A crystal possesses a center of symmetry when every point on the surface of the crystal has an identical point on the opposite side of the center, equidistant from it.

Example: cube

Page 43: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

If a crystal is rotated 360 about any given axis, it obviously returns to its original position.

If the crystal appears to have reached its original more than once during its complete rotation, the chosen axis is an axis of symmetry.

SYMMETRY ABOUT A LINE

Page 44: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

DIAD AXIS

TRIAD AXIS

TETRAD AXIS

HEXAD AXIS

AXIS OF SYMMETRY

• Rotated 180• Twofold rotation axis

• Rotated 120• Threefold rotation axis

• Rotated 90• Fourfold rotation axis

• Rotated 60• Sixfold rotation axis

Page 45: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

THE 13 AXES OF SYMMETRY IN A CUBE

Page 46: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

A plane of symmetry bisects a solid object in a such manner that one half becomes the mirror image of the other half in the given plane.

A cube has 9 planes of symmetry:

SYMMETRY ABOUT A PLANE

THE 9 PLANES OF SYMMETRY IN A CUBE

Page 47: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

Cube (hexahedron) is a highly symmetrical body as it has 23 elements of symmetry (a center, 9 planes, and 13 axis).

Octahedron also has the same 23 elements of symmetry.

Page 48: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

ELEMENTS OF SYMMETRY

Page 49: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

Combination forms of cube and octahedron

Page 50: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

IONIC

COVALENT

MOLECULAR

METALLIC

SOLID STATE

BONDING

• Composed of ions• Held by electrostatic force• Eg.: NaCl

• Composed of neutral atoms• Held by covalent bonding• Eg.: diamond

• Composed of molecules• Held by weak attractive force• Eg.: organic compounds

SOLID STATE BONDING

• Comprise ordered arrays of identical cations

• Held by metallic bond• Eg.: Cu, Fe

Page 51: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

ISOMORPH Two or more substances that crystallize in almost

identical forms are said to be isomorphous.

Isomorphs are often chemically similar.

Example: chrome alum K2SO4.Cr2(SO4)3.24H2O (purple) and potash alum K2SO4.Al2(SO4)3.24H2O (colorless) crystallize from their respective aqueous solutions as regular octahedral. When an aqueous solution containing both salts are crystallized, regular octahedral are again formed, but the color of the crystals (which are now homogeneous solid solutions) can vary from almost colorless to deep purple, depending on the proportions of the two alums in the solution.

Page 52: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

CHROME ALUM CRYSTAL

Page 53: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

A substance capable of crystallizing into different, but chemically identical, crystalline forms is said to exhibit polymorphism.

Different polymorphs of a given substance are chemically identical but will exhibit different physical properties, such as density, heat capacity, melting point, thermal conductivity, and optical activity.

Example:

POLYMORPH

Page 54: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

ARAGONITE

Page 55: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

CRISTOBALITE

Page 56: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

Polymorphic Forms of Some Common Substances

Page 57: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London
Page 58: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

Material that exhibit polymorphism present an interesting problem:

1. It is necessary to control conditions to obtain the desired polymorph.

2. Once the desired polymorph is obtained, it is necessary to prevent the transformation of the material to another polymorph.

Polymorph 1Poly-

morph 2

Polymorphic transition

Page 59: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

In many cases, a particular polymorph is metastable

Transform into more stable state

Relatively rapid infinitely slow

Carbon at room temperature

Diamond(metastable)

Graphite(stable)

Page 60: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

POLYMORPH

MONOTROPIC ENANTIOTROPIC

One of the polymorphs is the stable form at all

temperature

Different polymorphs are stable at different

temperature

The most stable is the one having lowest

solubility

Page 61: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

CRYSTAL HABIT

In nature perfect crystals are rare. 

The faces that develop on a crystal depend on the space available for the crystals to grow. 

If crystals grow into one another or in a restricted environment, it is possible that no well-formed crystal faces will be developed. 

However, crystals sometimes develop certain forms more commonly than others, although the symmetry may not be readily apparent from these common forms. 

The term used to describe general shape of a crystal is habit.

Page 62: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

Crystal habit refers to external appearance of the crystal.

A quantitative description of a crystal means knowing the crystal faces present, their relative areas, the length of the axes in the three directions, the angles between the faces, and the shape factor of the crystal.

Shape factors are a convenient mathematical way of describing the geometry of a crystal.

If a size of a crystal is defined in terms of a characteriza-tion dimension L, two shape factors can be defined:

Volume shape factor : V = L3

Area shape factor : A = L2

Page 63: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

Some common crystal habits are as follows.

Cubic - cube shapes

Octahedral - shaped like octahedrons, as described above.

Tabular -  rectangular shapes.

Equant - a term used to describe minerals that have all of their boundaries of approximately equal length.

Fibrous -  elongated clusters of fibers.

Acicular -  long, slender crystals.

Prismatic -  abundance of prism faces.

Bladed -  like a wedge or knife blade

Dendritic - tree-like growths

Botryoidal - smooth bulbous shapes

Page 64: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London
Page 65: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

Internal structure External habit ?=

Tabular Prismatic Acicular

External shape of hexagonal crystal displaying the same faces

Page 66: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

Crystal habit is controlled by:

1. Internal structure

2. The conditions at which the crystal grows (the rate of growth, the solvent used, the impurities present)

Variation of sodium chlorate crystal shape grown: (a) rapidly; (b) slowly

Page 67: Electronic structure Bonding State of aggregation Octet stability Primary: 1.Ionic 2.Covalent 3.Metallic 4.Van der Waals Secondary: 1.Dipole-dipole 2.London

(a) (b)

Sodium chloride grown from: (a) pure solution; (b) Solution containing 10% urea