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Organic Molecular Solids

   Prof. Allen M. Hermann
Professor of Physics Emeritus
    University of Colorado
   Boulder, Colorado USA
             and
      Vice-President
  NanoTech Solutions, Inc.
    Lexington, KY USA

allen.hermann@colorado.edu
Course Outline
Section I.
. Introduction
Materials, crystal structures

Prototypical Molecules, anthracene,
naphthalene, etc.

Molecular Solids

Materials Preparation

Electronic Properties Measurements
II. Insulators
Charge Transport Theory, narrow bands
Delocalized (Bloch) Wave Functions
Localized Wave Functions
Excitons
Peirels Distortion (1D systems)
III. Transient and Steady-state Photoconductivity in
Insulators, Theory and Experiment
 Small-signal limit
Drift Mobility
Trapping (shallow and deep)

IV. Effects of Finite Charge Injection
Boundary Conditions, Space Charge Limited Currents
Pulsed, Steady-state Electric Fields and Light
Excitations
Dispersive transport
V. Organic Conductors
Charge-transfer Complexes
Quasi-one-dimensional and two-dimensional
materials, radical-ion salts
Polymers
VI. Carbon-based nanostructures and
Superconductors
Buckyballs, Nanotubes, Graphene
Organic Superconductors
VII. Applications
Electrostatic Imaging and Xerographic materials
Organic Light-emitting diodes ) OLEDS and Active
Matrix OLEDS (AMOLEDS) for Display and Lighting
Solar Cells
Field-effect transistors
Batteries
Photo-detectors
Luminescence for Land-mine Sniffing
Lasers
Switches
E-Ink
Section I.
       . Introduction
 Materials, crystal structures
   Prototypical Molecules,
anthracene, naphthalene, etc.
      Molecular Solids
    Materials Preparation
    Electronic Properties
       Measurements
Conductivity
Of Organic
Materials
Bonds

Chapter 5 of Solymar
Introduction
• When two hydrogen atoms come close to each
  other
  – They form a chemical bond, resulting in a hydrogen molecule (H2)
• When many silicon atoms come close
  – They form many chemical bonds, resulting in a crystal
• What brings them together?
  – The driving force is




                      To reduce the energy
Interactions between Atoms

• For atoms to come close and form bonds, there must be
  an attractive force
   – Na gives up its 3s electron and becomes Na+
   – Cl receives the electron to close its n = 3 shell and becomes Cl-
   – The Coulomb attractive force is proportional to r-2
• In the NaCl crystal, Na+ and Cl- ions are 0.28 nm apart
   – There must be a repulsive force when the ions are too close to
     each other
   – When ions are very close to overlap their electron orbitals and
     become distorted, a repulsive force arises to push ions apart and
     restore the original orbitals
   – This is a short-range force
Equilibrium Separation
• There is a balance point, where the two forces cancel out (Fig.
  5.1)
   – The energy goes to zero at infinite separation
   – As separation decreases, the energy decreases, so the force is
     attractive
   – At very small separation, the energy rises sharply, so the force is
     strongly repulsive
   – The minimum energy point (Ec, or the zero force point) corresponds to
     the equilibrium separation ro
   – The argument is true for both molecules in crystals
Mathematical
• Mathematically
                                            A B
                                     E(r )  n  m
   – A and B are constants                  r r
   – The first term represents the repulsion and the second attraction
• Minimum energy
                                          B m
                                 EC      m
                                            (  1)
                                         ro n
   – It must be negative, so m < n
Bond Types
• Four types in total
   –   Ionic
   –   Covalent
   –   Metallic
   –   van der Waals
Metallic Bonds

• Each atom in a metal donates one or more
  electrons and becomes a lattice ion
  – The electrons move around and bounce back and forth
  – They form an “electron sea”, whose electrostatic
    attraction holds together positive lattice ions
  – The electrostatic attraction comes from all directions,
    so the bond is non-directional
  – Metals are ductile and malleable
Covalent Bonds
• When two identical atoms come together, a covalent bond
  forms
• The hydrogen molecule
   – A hydrogen atom needs two electrons to fill its 1s shell
   – When two hydrogen atoms meet, one tries to snatch the electron
     from the other and vice versa
   – The compromise is they share the two electrons
       • Both electrons orbit around both atoms and a hydrogen molecule
         forms
• The chlorine molecule
   – A chlorine atom has five 3p electrons and is eager to grab one more
   – Two chlorine atoms share an electron pair and form a chlorine atom
Group IV
• Carbon 1s22s22p2; Si 1s22s22p63s23p2; Ge
  1s22s22p63s23p63d104s24p2
• Each atom needs four extra electrons to fill the p-shell
   – They are tetravalent
• sp3 hybridization
   – s shell and p shell hybridize to form four equal-energy dangling
     electrons
   – Each of them pairs up with a dangling electron from a neighbor atom
   – There are four neighbor atoms equally spaced
   – Each atom is at the center of a tetrahedron
   – Interbond angle 109.4
   – Covalent bond is directional
Group IV

• At 0 K
   – All electrons are in bonds orbiting atoms
   – None can wander around to conduct electricity
   – They are insulators
• At elevated temperatures
   – Statistically, some electrons can have more enough energy to
     escape through thermal vibrations and become free electrons
   – They are semiconductors
• The C–C bond is very strong, making diamond the hardest
  material known (Table 5.1)
   – Diamond has excellent thermal conductivity
   – It burns to CO2 at 700C
van der Waals Bonds
• Argon has outer shell completely filled
• When argon is cooled down to liquid helium temperature, it
  forms a solid
   – The electrons are sometimes here and sometimes there, so the
     centers of the positive charge (nucleus) and negative charge
     (electrons) are not always coincident
   – The argon atom is a fluctuating dipole (instantaneous dipole)
   – It induces an opposite dipole moment on another argon atom, so they
     attract each other
   – Such attraction is weak, so the materials have low melting and boiling
     temperatures
   – They are often seen in organic crystals
Aromatic Hydrocarbon Bonds
Conducting Organic Materials
Extreme Case – Nearly Ionic Bonds
 in Highly Conducting Complexes

     “Charge Transfer salts”
Discovery of Conducting Organic Crystals
Materials Preparation
    Techniques
S   S   S   S

S   S   S   S
Electronic Measurements
Conductivity (Resistivity)
Conductivity s = enm
n: number of carriers; m: mobility of the carriers
4-probe resistivity measurement
Van Der Pauw resistivity measurement
Hall effect
Drift Mobility from Time of
Flight Measurements and TFT
         Structures
Some references to this material
Section 1 oms
Section 1 oms
Section 1 oms

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Section 1 oms

  • 1. Organic Molecular Solids Prof. Allen M. Hermann Professor of Physics Emeritus University of Colorado Boulder, Colorado USA and Vice-President NanoTech Solutions, Inc. Lexington, KY USA allen.hermann@colorado.edu
  • 3. Section I. . Introduction Materials, crystal structures Prototypical Molecules, anthracene, naphthalene, etc. Molecular Solids Materials Preparation Electronic Properties Measurements
  • 4. II. Insulators Charge Transport Theory, narrow bands Delocalized (Bloch) Wave Functions Localized Wave Functions Excitons Peirels Distortion (1D systems)
  • 5. III. Transient and Steady-state Photoconductivity in Insulators, Theory and Experiment Small-signal limit Drift Mobility Trapping (shallow and deep) IV. Effects of Finite Charge Injection Boundary Conditions, Space Charge Limited Currents Pulsed, Steady-state Electric Fields and Light Excitations Dispersive transport
  • 6. V. Organic Conductors Charge-transfer Complexes Quasi-one-dimensional and two-dimensional materials, radical-ion salts Polymers VI. Carbon-based nanostructures and Superconductors Buckyballs, Nanotubes, Graphene Organic Superconductors
  • 7. VII. Applications Electrostatic Imaging and Xerographic materials Organic Light-emitting diodes ) OLEDS and Active Matrix OLEDS (AMOLEDS) for Display and Lighting Solar Cells Field-effect transistors Batteries Photo-detectors Luminescence for Land-mine Sniffing Lasers Switches E-Ink
  • 8. Section I. . Introduction Materials, crystal structures Prototypical Molecules, anthracene, naphthalene, etc. Molecular Solids Materials Preparation Electronic Properties Measurements
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  • 18. Introduction • When two hydrogen atoms come close to each other – They form a chemical bond, resulting in a hydrogen molecule (H2) • When many silicon atoms come close – They form many chemical bonds, resulting in a crystal • What brings them together? – The driving force is To reduce the energy
  • 19. Interactions between Atoms • For atoms to come close and form bonds, there must be an attractive force – Na gives up its 3s electron and becomes Na+ – Cl receives the electron to close its n = 3 shell and becomes Cl- – The Coulomb attractive force is proportional to r-2 • In the NaCl crystal, Na+ and Cl- ions are 0.28 nm apart – There must be a repulsive force when the ions are too close to each other – When ions are very close to overlap their electron orbitals and become distorted, a repulsive force arises to push ions apart and restore the original orbitals – This is a short-range force
  • 20. Equilibrium Separation • There is a balance point, where the two forces cancel out (Fig. 5.1) – The energy goes to zero at infinite separation – As separation decreases, the energy decreases, so the force is attractive – At very small separation, the energy rises sharply, so the force is strongly repulsive – The minimum energy point (Ec, or the zero force point) corresponds to the equilibrium separation ro – The argument is true for both molecules in crystals
  • 21. Mathematical • Mathematically A B E(r )  n  m – A and B are constants r r – The first term represents the repulsion and the second attraction • Minimum energy B m EC  m (  1) ro n – It must be negative, so m < n
  • 22. Bond Types • Four types in total – Ionic – Covalent – Metallic – van der Waals
  • 23. Metallic Bonds • Each atom in a metal donates one or more electrons and becomes a lattice ion – The electrons move around and bounce back and forth – They form an “electron sea”, whose electrostatic attraction holds together positive lattice ions – The electrostatic attraction comes from all directions, so the bond is non-directional – Metals are ductile and malleable
  • 24. Covalent Bonds • When two identical atoms come together, a covalent bond forms • The hydrogen molecule – A hydrogen atom needs two electrons to fill its 1s shell – When two hydrogen atoms meet, one tries to snatch the electron from the other and vice versa – The compromise is they share the two electrons • Both electrons orbit around both atoms and a hydrogen molecule forms • The chlorine molecule – A chlorine atom has five 3p electrons and is eager to grab one more – Two chlorine atoms share an electron pair and form a chlorine atom
  • 25. Group IV • Carbon 1s22s22p2; Si 1s22s22p63s23p2; Ge 1s22s22p63s23p63d104s24p2 • Each atom needs four extra electrons to fill the p-shell – They are tetravalent • sp3 hybridization – s shell and p shell hybridize to form four equal-energy dangling electrons – Each of them pairs up with a dangling electron from a neighbor atom – There are four neighbor atoms equally spaced – Each atom is at the center of a tetrahedron – Interbond angle 109.4 – Covalent bond is directional
  • 26. Group IV • At 0 K – All electrons are in bonds orbiting atoms – None can wander around to conduct electricity – They are insulators • At elevated temperatures – Statistically, some electrons can have more enough energy to escape through thermal vibrations and become free electrons – They are semiconductors • The C–C bond is very strong, making diamond the hardest material known (Table 5.1) – Diamond has excellent thermal conductivity – It burns to CO2 at 700C
  • 27. van der Waals Bonds • Argon has outer shell completely filled • When argon is cooled down to liquid helium temperature, it forms a solid – The electrons are sometimes here and sometimes there, so the centers of the positive charge (nucleus) and negative charge (electrons) are not always coincident – The argon atom is a fluctuating dipole (instantaneous dipole) – It induces an opposite dipole moment on another argon atom, so they attract each other – Such attraction is weak, so the materials have low melting and boiling temperatures – They are often seen in organic crystals
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  • 38. Extreme Case – Nearly Ionic Bonds in Highly Conducting Complexes “Charge Transfer salts”
  • 39. Discovery of Conducting Organic Crystals
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  • 44. Materials Preparation Techniques
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  • 48. S S S S S S S S
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  • 52. Conductivity s = enm n: number of carriers; m: mobility of the carriers
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  • 55. Van Der Pauw resistivity measurement
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  • 60. Drift Mobility from Time of Flight Measurements and TFT Structures
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  • 69. Some references to this material