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Nanowires
Course outline
1
Introduction
2
Theoretical background
Biochemistry/molecular biology
3
Theoretical background computer science
4
History of the field
5
Splicing systems
6
P systems
7
Hairpins
8
Detection techniques
9
Micro technology introduction
10
Microchips and fluidics
11
Self assembly
12
Regulatory networks
13
Molecular motors
14
DNA nanowires
15
Protein computers
16
DNA computing - summery
17
Presentation of essay and discussion
Introduction
Molecular electronics
www.scientificamerican.com
Molecular electronics
Biological Systems
Molecular Electronics Devices
Use molecular electronics to study biological systems.
Molecular electronics
Incentives

 Molecules are nano-scale
 Self assembly is achievable
 Very low-power operation
 Highly uniform devices
Quantum Effect Devices

 Building quantum wells using molecules
Electromechanical Devices

 Using mechanical switching of atoms or molecules
Electrochemical Devices

 Chemical interactions to change shape or orientation
Photoactive Devices

 Light frequency changes shape and orientation.
Molecular electronics
Definition
is a field emerging around the premise that it
is possible to build individual molecules that
can perform functions identical to those of
the key components of today’s microcircuits.
Why molecular electronics?
Chip-fabrication
specialists
will
find
it
economically infeasible to continue scaling
down microelectronics.
 stray signals on the chip
 the need to dissipate the heat from so many

closely packed devices
the difficulty of creating the devices in
the first place
Molecular electronics, any better?

Modern technologies can only go so far.

Solution (new development)
 DNA - It is promising to achieve
super-high density memory and high
sensitive detection technology.
 Cell Computing

Silicon transistors at 120 nm in length
will still be 60,000 times larger in area
than molecular electronic devices.
Recent research

Recent studies have shown that individual
molecules can conduct and switch electric
current and store information.

July of 1999 – HP and the University of
California
at
Los
Angeles
build
an
electronic switch consisting of a layer
of
several
million
organic
substance
molecules
of
an
called
rotaxane.
Linking a number of switches version of an AND gate is produced.
a
Recent research
June 2002 - Fuji Xerox biotechnology made
a prototype transistor of DNA from salmon
sperm.

Researchers
successfully
passed
an
electric
current
through
the
DNAtransistor.

This
demonstrates
that
behaves
in
a
similar
semiconductor.

Super smaller chip in 10 years.
the
chain
fashion
to
Recent research
Atomic force microscope image of semi-conductive DNA compound
http://www.fujixerox.co.jp/research/eng/category/inbt/m_electronics/index.html
Self assembly
Molecular self-assembly

the
autonomous
organization
of
components into patterns or structures
without human intervention (Whitesides
2002)

Current Problem: Forming electrical
interconnects between molecules
Self assembly
www.scientificamerican.com
Molecular electronics
Thiol
Acetylene linkage
Benzene ring
Molecular electronics

Mechanical synthesis
 Molecules aligned using a scanning tunneling
microscope (STM)
 Fabrication done molecule by molecule using
STM

Chemical synthesis
 Molecules
aligned
in
interactions
 Self assembly
 Parallel fabrication
place
by
chemical
an atomic relay
A very short
Electronics course
Transistors
A device composed of semiconductor
material that amplifies a signal or
opens or closes a circuit. Invented in
1947 at Bell Labs, transistors have
become
the
key
ingredient
of
all
digital circuits, including computers.
Today's microprocessors contains tens
of millions of microscopic transistors.
Transistors
Transistors consist of three terminals; the source, the gate,
and the drain.
Transistors
In the n-type transistor, both the source and the drain are
negatively-charged and sit on a positively-charged well of psilicon.
Transistors
When positive voltage is applied to the gate, electrons in the
p-silicon are attracted to the area under the gate forming an
electron channel between the source and the drain.
Transistors
When positive voltage is applied to the drain, the electrons
are pulled from the source to the drain. In this state the
transistor is on.
Transistors
If the voltage at the gate is removed, electrons aren't
attracted to the area between the source and drain. The
pathway is broken and the transistor is turned off.
DNA wires
DNA

Well known from biology

Forms predictable structure

Controllable
self
assembly
through base pair sequences

May be selectively processed
using restriction enzymes
http://www.chemicalgraphics.com/
DNA in microelectronics

As
the
major
component
in
a
Single
Electron Tunneling (SET) Transistor

As tags to connect up nano-circuitry
including wires and nanoparticles (taking
advantage of DNA selectivity)

As
basis
for
computation)
a
Qubit
(for
quantum
DNA SET transistor
DNA
Single electron transistor
Main strand
Gate strand
Equivalent Electrical Circuit
E. Ben-Jacob , Phys. Lett. A 263, 199 (1999).
Main strand
Assumptions

Chemical bonds(in DNA) can act as
tunnel
junctions
in
the
coulomb
blockade
regime,
could
emit
electricity, given a proper coating.

Has the ability to coat a DNA strand
with metal in nanometer scale.
Operation
Schematic image with 2 grains in DNA connected by
P-bond. Dark circle->carbon atoms, white circles>oxygen atoms.
DNA pairs

P-bond
-> tunneling junction.

H-bonds
-> capacitor.

The grain itself -> inductive properties.
DNA pairs



P bond: Has 2  bonds, 1  bond.
The  electron can be shared with 2 oxygen,
resembles an electron in well, put it on the
lowest level.
When electron enters, it meet the barrier set
by energy gap.

But the gap is narrow and
electron can walk trough.
small
so
the
DNA pairs

H-bonds: Can be the capacitor.

The proton in the h-bond can screen a net charge
density on either side, by movement.

Thus the net charge could be in the side of the h-bond.

The grains: Can be the inductive properties.

Due to the hopping of additional electrons.

But can be ignored (L & Lo is small, consistent to the
usual SET)
DNA pairs

Consist of 2 strands (1 main, 1 gate)

Connect the end base of the gate strand with a
complimentary strand.

Both strands should be metal-coated, except (a)
the grain in the main strand, which connect to the
gate strand, the
connective h-bond.

2
adjacent
P-bonds,
(b)
Connect the main strand with voltage source (V)
the
DNA pairs
The end of the gate strand with another voltage source
(Vg) that acts as gate source.
Functionalisation of nanoparticles

DNA may be attached to surface area
of
nanoparticles
to
construct
desired assemblies.

May provide insight to possible
solution to connecting transistors
Functionalisation of nanoparticles
Mirkin et al.: Nature, 1996, 382, 607
Functionalisation of nanoparticles
Mirkin et al.: Nature, 1996, 382, 607
Functionalisation of nanoparticles
8 nm gold particles attached to a 31 nm gold particle with DNA
http://www.chem.nwu.edu/~mkngrp/dnasubgr.html
DNA conductance

Double helix – a backbone and base pairs

Building
blocks
A, T, C & G

Example: 10 base pairs per turn, distance of
3.4 Angstroms between base pairs.

Arbitrary sequences possible

A challenge for nanotechnology is controlled /
are
the
base
pairs:
reproducible growth. DNA is an example with
some success. However, there are many copies in
a solution!

2D and 3D structures with DNA base pairs as a
building block have been demonstrated

Lithography? Not yet.
DNA base-pairs
DNA conductance

Conductivity in DNA has
been controversial

Electron transfer experiments (biochemistry) /
possible link to cancer

Transport experiments (physics)
DNA conductance
Metallic, No gap
Current
Current
~ 1nA
~ 10nA
Semiconducting / Insulating
Voltage (V)
Porath et. al, Nature (2000)
Voltage 20mV
Fink et. al, Science (1999)
Counter-ions

Is conduction through the base
pair or backbone? - Basepair

When DNA is dried, where are the
counter ions?

Crystalline / non crystalline?

Counter ions significantly modify
the energy levels of the base
pairs

Counter-ion
important

Resistance
species
increases
is
also
with
length
of
the
DNA
(exponential within the
of simple models)
the
sample
context
Counter-ions
DNA-based metalised nanowires
10 nm wires:
AuPd on DNA
Needed

Smaller wires and constructs

Difficult to make
conventional means

Find
if
DNA
is
wires
a
good
this
scale
substrate
metalisation (and for which metals)

Conducting and superconducting wires
by
for
Which DNA?

λ-DNA:
double-stranded,
2 nm width, 16 micron
length

Poly-C,
Poly-A,
etc.:
Single-stranded, all same
base, 1 nm width

Designed,
complementary
strands:
Self assembly
presents possibility for
complex structures
λ-DNA, uncoated:
~5 nm wires
Metalised DNA
1)
2)

Earlier construction of DNA-templated nanowires

Braun

Richter

Nanotubes, other substrates
1:
100 nm thick wires, Ag on DNA
2:
50 nm thick wires, Pd on DNA
E. Braun, Y.Eichen, U. Sivan, and G. Ben-Yoseph, Nature (London) 391, 775 (1998).
J. Richter et al. Appl. Phys. Lett. 78, 536 (2001)
Methods
Suspend DNA across undercut 100 nm trench
-or

Suspend
across
cuts in
thin (60 nm)
membrane –variable width carved by focused
ion beam

Metalize by sputtering or evaporation

Image with scanning electron microscope

Make electrical measurements
Methods
Schematic of undercut trench
Set-up
Schematic of electrode overlaying wire
Methods
Hitachi 4700 Scanning Electron Microscope
More metalised DNA-wires
AuPd sputtered on λ DNA
Osmium plasma coated on λ DNA

Wires made repeatedly, variety of coatings (or none)

Width range from <5 nm bare DNA wires to >30 nm heavily
coated in AuPd. The thinnest contiguous wires are ~10 nm
thick
Metalised DNA-wires
Variable width cuts in membrane, made by focused ion beam. DNA
bridges the cuts.


Longest wire to date: 960 nm (~30 nm thick)
Appearance of multi-strand “Ropes”
Metalised DNA-wires
Multi-strand “rope,” 3 nm AuPd
coating,
total thickness: 3040 nm Length: 960 nm
Two wires connected by “rope”
visible on surface of membrane,
length: 550 nm on right, 670 nm
on left
Is it functional?

Measurement contacts produced
photolithography techniques
by

Potentially superconducting
or 3He system

First Mo0.79Ge0.21 coated samples:
superconductivity
standard
samples
in
4He
test for
Not yet ....

First MoGe sample weakly conductive,
superconductivity- too thin!

Room temperature:
2.3 MΩ, Lowest point:
750 kΩ, sharp upturn near usual critical
temperature (near 4 K)

Possible
film

Next samples:
Si coat
discontinuities
or
oxidation
no
of
7 nm MoGe with protective
Variations

More conductivity measurements

Different DNA structures

Normal and

Device possibilities?

As thin as possible (preferably
functional)
superconducting wires
Variations
Poly-C wire with 2 nm AuPd, total width: 5 nm.
DNA template
DNA templated electronics
The DNA acts as a scaffold for positioning a
single-walled carbon nanotube at the heart of
a field-effect transistor, as well as a
template for the metallic wires connecting
the device.
K Keren et al. 2003 Science 302 1380
DNA templated electronics
DNA templated electronics
What do we need to realise this

assemble a DNA network

localise moleculra scale electronic components

transform DNA into conducting wires
DNA templated wires
silver wires
formed on aldehyde derivitesed DNA
continuous gold wires
DNA templated gold wires
wire width ~50nm
DNA width ~2nm
R~26 Ω
Sequence specific molecular lithography
Sequence specific molecular lithography
RecA polymerised on DNA (cryo-TEM)
3-armed junction formation
building blocks
synapsis
final product
branch migration
AFM image of 3-armed junction
Sequence specific molecular lithography
patterning of DNA metallization
Sequence specific molecular lithography
Sequence specific molecular lithography
RecA nuleoprotein filament
localised on aldehydederivatized DNA
sample after silver deposition
AFM
sample after gold deposition
SEM
Sequence specific molecular lithography
optical lithography
molecular lithography
Others
Carbon nanotubes
Carbon nanotubes
The device - which consists of
a single-walled carbon nanotube
sandwiched
between
two
gold
electrodes
operates
at
extremely
fast
microwave
frequencies.
The
result
is
an
important step in the effort to
develop
nanoelectronic
components that could be used
to replace silicon in a range
of electronic applications (S
Li et al. 2004 Nano Lett. 4
753).
http://physicsweb.org/article/news/8/4/15
Superconductivity in nanotubes

Left red data show insulating like behavior with
resistance upturns at the lowest temperatures, blue data
show superconducting behavior

Right V-I data for a strongly superconducting sample at
various temperatures.
Courtesy, A. Bollinger
Buckyball
www.osti.gov/accomplishments/ smalley.html
Cellular computing
Cellular computing
Goals

To use a cell as the smallest DNA-based
molecular computer

More specifically, to mimic some or all
of a cells mechanisms in order to
produce
a
quasi
molecular
(QMC), or a true molecular
(TMC)
computer
computer
Quasi cellular computing

Most of the input and output operations are
driven by an external force
 Input
and programming provided, QMC
provides output
 All
molecular computers are of this
type, with the exception of the cell

Goal for QMC’s: to develop QMC’s that are
more efficient, and less dependent on
outside interaction
True cellular computing

“All
computational
operations
(input,
output, state transitions) are driven by
self organizing chemical reactions” (Ji
1999)
 All processes are internally driven, no
outside help is needed
 Only known example is a cell

Goal for TMC’s: to fabricate an artificial
TMC with the properties of a living cell
Cells versus computers
Qualities of cells that are
similar
to
those
in
computers

Have
inputs,
state
transitions, and outputs
as indicated by their
programming

Have
a
language
to
communicate between cells

Have
information
and
energy
storage
mechanisms: IDS’s
http://www.rkm.com.au/CELL/
Cells versus computers
Cells
Computers
Current carried by: Chemicals
Wires
Reactions or
Enzymes
processes turned on
or off by:
Transistors
Information stored
in:
Capacitors
Biopolymers,
IDS’s
Computational
DNA
programs stored in:
Software
Cells versus computers
Cells
Computers
Programmability No- not yet
Yes
SelfYes
Reproducibility
No- not yet
Ji, Sungchul. The Cell as the Smallest DNA Based Molecular Computer. BioSystems (1999):52 123-133.