introduction to molecular electronics2009...
TRANSCRIPT
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Introduction to MolecularIntroduction to Molecular Electronics
Lecture 1Lecture 1
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Conductive organic molecules
“Plastic can indeed, under certain circumstances, be made to behave very like a metal a discovery for which Alan J Heeger Alan Gvery like a metal - a discovery for which Alan J. Heeger, Alan G. MacDiarmid and Hideki Shirakawa are to receive the Nobel Prize in Chemistry 2000”.
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Why Molecular Electronics?• Low-cost devices (OLED, RF-ID,
chemical sensors etc.)• Beyond the Moor’s law: more devices
per unit area and not only• Self assembly: new old way to• Self-assembly: new old way to
assemble complicated devices• Complex (designer) logical functionsp ( g ) g• Interacting with living organisms: e.g.
linking biological functions and l t i d telectronic readout
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Molecular electronics approach MolecularElectronicsElectronics
Bulk Molecular Systems
Single MolecularSystems
El t i d i b d l l
y y
• Electronic devices based on molecules with specific conductance properties (e.g. OLEDs)Ch t i ti di i l• Characteristic dimensions are large compared with the size of a molecule
• Huge ensemble of molecules is contacted by usually inorganic electrode. Molecules are not individually addressable
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Molecular electronics approach• Single molecular systems
aim at individual contact to i l l l llsingle molecules or small
arrays of perfectly ordered moleculesmolecules
• HME: organic molecules are directly connected byare directly connected by inorganic electrodes (and eventually gates)
• MME: molecules are individually connected to each other forming a circuit. Electrodes are only used for data exchange and tofor data exchange and to supply energy
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Molecular building blocksDouble bond: sp2 hybridization
Single bond: sp3 hybridization
AO f i hb i b• Carbon atom can form four σ-bonds. • Free rotation is possible
i h i i f
p-AO of neighboring carbon atoms form π-bonding Rigid bond, length of 134 pm
with activation energy of 0.1 eV.• Bond length 154 pm
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Molecular building blocks• Molecules with more than one
double bond called polyenes.• Shape and properties of the
molecule depend on the position of Isolated double bondsp pthe double bond
• Conjugated double bonds play aConjugated double bonds play a particular role as π-electrones are delocalized over the extent of the
Conjugated double bonds
delocalized over the extent of the conjugation
Cumulated double bonds
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Molecular building blocks
• Cyclic polyenes with conjugation that spreads the entire ring are called aromatic or arenes
• Stability and delocalization of π-electrones is maintained in fusedelectrones is maintained in fused rings (polycyclic aromatic molecules))
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Molecular building blocks• Molecules with smaller or larger rings or other atoms in the
ring (heterocycles) possess the same delocalization i if h b f l i iproperties if the number of π-electrons is six.
Cyclapentadiene aniony p
Cyclaheptatriene cation
Heterocycles
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Molecular building blocks
• Molecules with a triple bond pare called alkynes
• Here, the π-electrons form aHere, the π electrons form a cylindrical cloud around σ-bondbond
• Very rigid, linear bond with the length of 120 nmthe length of 120 nm
• Conjugated triple bonds sho the same Acetyleneshow the same delocalization as double bonds
y
bonds
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Molecular wires• Molecular wires are, generally, rod-like structures with delocalized p-system,
the longer the structure the lesser the difference between the frontier orbitals and the Fermi level of the electrode
• polyene – alternating system of single and double bonds;;
• polythiophene
• polyphenylenevinylene
• polyphenyleneethynylene
• thyophenylsubstituted benzene
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Molecular insulator (spacer)• insulating molecular structures could be used as spacers i.e. have to be
significantly insulating to preserve energy difference, but still allow tunneling. g
• alkanes – good insulating properties, lack rigidity; g y
• adamantyl cage – good rigidity and insulating properties, synthetically demandingg
• tetramethylsubstituted bephenyl - single bonding connecting two rings with perpendicular p-systems
torsion angle is important perpendicular p systems
• metal-organic insulator (?)
• meta connected aromatic are insulators relative position is
opposite to ortho- and para- connections pimportant
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Electron in a box: example
• Electrons are sufficiently delocalized in yconjugated molecules that they can be considered as an electron boxconsidered as an electron box
• Electronic absorption of β-carotene
0.294nm
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Particle in a box
• The technique:– Solve Schrodinger equation
between the walls (V=0)I b d diti t th– Impose boundary condition at the walls and find the coefficients
2
2ˆ ˆ
2H E H
m xψ ψ ∂= = −
∂2m x∂2 2
2ikx ikx
k kkAe Be E
mψ −= + =
(0, ) 0k Lψ =
( ) i ( / ) 1 2C L( ) sin( / ) 1,2,...n x C n x L nψ π= =
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Particle in a box: example
• Electronic absorption of β-carotenep β
0.294nm
22 electrons fill states up to n=11
2
( )( )2
2 212 11 1
8hE E E n nmL
Δ = − = + −
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Peierls distortion• 1D delocalized
system is expectedsystem is expected to be metallic, however lowering energyhowever
• Monoatomic metallic h i ill d
g gy
chain will undergo a metal-insulator t iti t ltransition at low temperature;
• period doubling leads to opening a gap at π/2
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Peierls distortion
• Peierls transition in polyacetylene
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Charge-transfer complexes• Charge transfer compounds are formed by two or more types of neutral
molecules one of which acts as a donor and the other is an electron acceptorp
D A D A+• −•⎡ ⎤ ⎡ ⎤+ ⎯⎯→⎣ ⎦ ⎣ ⎦
Mixed stacks: not highly conductive
Segregated stacks: strong p-overlap results in delocalizing and high conductivity
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Charge-transfer complexes• Example: pyrene (10-12 S·m-1)
and iodine (10-7 S·m-1) form aand iodine (10 S m ) form a high conductivity complex with 1 S·m-11 S m .
E l• Example: TTF (tetrathiafulvalene) and TCNQ (tetracyanoquinodimethane)(tetracyanoquinodimethane)
• 1:1 mixture shows conductivity of about 5·102 S·m-1 and metallicabout 5 10 S m and metallic behaviour below 54K.
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Doping of organic semiconductors
• As in inorganic semiconductors, impurities can be g padded to either transfer an electron to LUMO (p*) or remove electron from HOMO (p).
[ ] ( ) ( )2 332
y
n y n
nyCH I CH I+ −⎡ ⎤+ ⎯⎯→⎢ ⎥⎣ ⎦
[ ] ( )2 y n
y
n nCH nyNa CH Na− +
⎣ ⎦
⎡ ⎤+ ⎯⎯→⎣ ⎦
• Large doping concentration is required 1-50%• Counter ions are fixed while charge on the polymer• Counter ions are fixed while charge on the polymer
backbone is mobile
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Quantum Mechanical Tunneling
• the wave nature of electrons allows penetration into a pforbidden region of the barrier
• at low voltages (V<<barrier height):at low voltages (V barrier height):
exp( )A Bdσ = −exp( )A Bdσ = −
• at higher voltages the barrier tilt should be taken intoat higher voltages the barrier tilt should be taken into account:
202 exp( )sinh
sin( ) 2CkT CVI I BV
CkTππ
⎡ ⎤ ⎛ ⎞= − ⎜ ⎟⎢ ⎥ ⎝ ⎠⎣ ⎦
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Molecules and contacts
Contact Contact
Molecule
M l l d t t f t ti l
Molecule
• Molecules and contacts form two essential parts of a molecular device.
• The contact of a molecule and bulk material is complicated strongly influence devicecomplicated, strongly influence device behaviour and only recently became a focus of intensive researchof intensive research
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Molecules and contacts
M l l b t t d i• Molecules can be contacted using:– Covalent bonds mechanically stable, short, allow
overlap of molecular orbitals and delocolized states in the metalExamples: Au-thiol, Au-CN, Pt-amine etc.
– Van der Waals interaction (e.g. Langmuir-( g gBlodgett film deposited on a substrate): wave functions don’t overlap, electron transport goes via p, p gtunneling to and from the molecule.
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Bond length effect
• If the distant is short enough that delocalized e d s a s s o e oug a de oca edstate of the molecule overlaps with the metallic electronic states than the common delocalizedelectronic states, than the common delocalized state is formed and electron can be t itt d th h th ttransmitted through the system.
• If the overlap is not achieved the wave function pcan be treated independently and the whole situation can be modeled as tunneling of ansituation can be modeled as tunneling of an electron from electrode to a molecule.
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Theory considerations: Contacts and MO overlapt ib ti f diff t MO t th t t l• contribution of different MO to the current may very strongly
depending on their spatial arrangement• issue of contact is important: a “supermolecule” involving last p p g
few metal atoms should be in the calculations
HOMO: depleted at the contacts
LUMO: depleted in the middle
l l i MO ( 1 V) ilower lying MO (~1eV) is important for current
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Role of contacts
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Molecular device
Contact Contact
MoleculeMolecule
• what type of behaviour we can expect for a complete s stem?complete system?
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Ballistic conductorContacts of finite transparency
µ1
µ2
• The model:– Electrons tunnel with some probability (contact
transparency) into the channel– Transport is coherent – Contacts are ”reflectionless”
• The question:q• What is the resistance of the channel? Where the heat is
dissipated?
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Ballistic conductor model
• Electrons moving from left to right haveElectrons moving from left to right have potential µ1, from right to left µ2.
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Quantized conduction of a ballistic conductorTh it ti fi t t d i 2DEG t B J• The situation was first encountered in 2DEG system, e.g. B.J. van Wees et al, Phys Rev. Lett. 60, 848 (1988).
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Theory considerations: Resonance transport
• Landauer-Buttiker theory: electron is a daue u e eo y e ec o stransmitted through a state with a certain probability (transparency) Tr(t t’)probability (transparency) Tr(t,t )
electron states in the molecule
EF
electrodes
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• Coherent conductance is expected to Co e e co duc a ce s e pec ed ocharacterize most of short molecular wires. The cond ctance is gi en• The conductance is given:
22e,
2( , ) ( , )iji j
eg E V t E Vh
= ∑Probability to go from the transverse mode i in the left contact to the transverse mode j in the right contact
Quantum of conductance
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Variable range hopping
• for disordered materials the charge transfer goes by a process similar to diffusion as the mean free path is of the order of interatomic distance
1/ 4⎛ ⎞
• Mott equation 1/3 for 2D and ½ for 1D1/3 for 2D and ½ for 1D
1/ 40
0 exp TT
σ σ⎛ ⎞⎛ ⎞= −⎜ ⎟⎜ ⎟⎜ ⎟⎝ ⎠⎝ ⎠⎝ ⎠
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Shottky and Poole-Frenkel effects• Barrier can be created at the interface due to charge re-
distribution (Shottky barrier)
0.5
exp EJkTβ⎛ ⎞
∝ ⎜ ⎟⎝ ⎠kT⎝ ⎠
Fowler-Nordheim tunneling
2 expJ E γ−⎛ ⎞∝ ⎜ ⎟
Fowler-Nordheim tunneling
expJ EE⎜ ⎟
⎝ ⎠
Poole-Frenkel effect
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Theory considerations: Coulomb blockade
• Charging effects on the nanoscale are importantg g p
Geometrical effect:d d h i l idepends on the particle size and geometry of the contacts
1nm cluster: Ec ~ 0.5 eV
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Design Challenges for Molecular Circuits
≠≠• Applicability of superposition principle is
restricted as molecular parts can not be ptreated independently. Effect of molecular structure on density of states and geometry of y g yMO should be considered
• Coulomb blockade effects: conductance will• Coulomb blockade effects: conductance will depend on charge on subunits and the capacitance to the gatecapacitance to the gate
• Interference effects
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Experimental challenges
• The challenges:g–how to attach molecules to the
l t delectrodes–how to arrange them in the same–how to arrange them in the same
direction