MEMS &NEMS and Molecular Engineering
Dr.Marc Madou Chancellor’s Professor UC Irvine Tsukuba, February 28 , 2005 Outline of Presentation
Two Approaches to Miniaturization
Biomimetics: Icarus Revisited?
Applications:
Move to Point of Care (POC) with DNA Arrays on a CD
Nanomanipulator Platform-Beyond Moore’s Law
Responsive Drug Delivery-Smart Pills
C-MEMS
Conclusions Two Approaches to Miniaturization
Nanomachining (top-down) is an extension of micromachining:
EUV (13.4 nm) ⇑
Very thin resists including SAM’s
Surface imaging resists
Phase shift masks
X-ray lithography⇓
3D instead of 2-D
Soft-lithography
Proximal tool writing
Harold Craighead Cornell Two Approaches to Miniaturization
Nanochemistry (bottom-up) is a biomimetic approach to make nanodevices :
Self assembly
Crystals
Langmuir-Blodgett monolayers and multilayers on solids
Self-assembled monolayers (SAM) (e.g., thiols on Au, silanes on SiO2) Mechanosynthesis with proximal probes Hints: flexible instead of stiff materials, C instead of Si (C-MEMS), self-assembly (SAM), massive parallelism, writing with nano- particles, make hybrids of top-down (e.g., proteins, DNA) and bottom-up (e.g., fluidic platforms) http://www.almaden.ibm.com/vis/stm/atomo.html Biomimetics: Icarus Revisted?
Nature and mankind have developed competitive manufacturing methods on the macro level (e.g., steel versus bone) Biomimetics on the macro-level mostly failed. Background reading: Cats’ Paws and Catapults by Steven Vogel (Efficiency of mechanical systems in biology and human engineering in the macro-world). On the nanoscale nature is outperforming us by far (perhaps because nature has had more time working towards biological molecules/ cells than towards making larger organisms such as trees and us). NEMS might be inspired by biology but will most likely be different again -- the drivers for human and natural manufacturing techniques are very different. Move to Point of Care (POC) with DNA Arrays on a CD
Memory devices today and tomorrow
Molecular diagnostics today and tomorrow
DNA bacteria, Hybridization Raw sample RNA cancer cell, Electrophoresis WBC, et al protein Sequencing Cell Cell Lysis, Amplification Separation Purification
Sample Preparation Move to Point of Care (POC) with DNA Arrays on a CD
Nanogen’s active DNA array (100, 400, 10,000 sites)
Transport
Addressing
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Stringency
Improvements needed: make much smaller, merging with sample preparation, and avoid desalting while maintaining speed of hybridization reaction
QuickTime™ and a Cinepak decompressor are needed to see this picture.
10,00010,000-Site-Site CMOSCMOS ChipChip Move to Point of Care (POC) with DNA Arrays on a CD Instrument Fluidics Power Mechanical pressure Propulsion Electrokinetics (AC and Heater (PCR) DC) Electronics Centrifuge Detection
(Acoustic)
Disposable Cassette Reagents Fluidics PROPULSION
Mechanical pressure Acoustic Centrifugal Electrokinetic Move to Point of Care (POC) with DNA Arrays on a CD
Closed Chip Electrokinetic (DC) 2 l
Fluid contact
First products (Caliper)
Not generic
May solve liquid valving but not for vapors !
Mixing difficult to implement
Many parameters influence propulsion force
High voltage source is not convenient
Better for high-throughput screening and smaller samples Move to Point of Care (POC) with DNA Arrays on a CD
Centrifugal 3 l
No fluid contact
Established
Generic
Solves liquid valving elegantly
Widest dynamic range
Simple and inexpensive CD player for drive
Mixing easy to implement QuickTime™ and a YUV420 codec decompressor Most functions are needed to see this picture. demonstrated
Cell work easier
Sample preparation easier
Better for diagnostics Move to Point of Care (POC) with DNA Arrays on a CD
Center Software code enables us to design quickly simple fluidic elements on the CD. Now we
R1 are focusing on implementing porous materials on the CD (e.g., for a separation r column). Modeling is much harder here. R2 dP c = ρω 2 r θ dr ω R + R ∆P = ρω 2(R − R ) 2 1 = ρω 2∆R ⋅ R c 2 1 2 γ cos θ ⋅ C ∆ P = s A 1 1 γ cosθ ⋅C 2 γ cosθ 2 fb ≥ ( 2 ) = ( 2 ) π ρ⋅ R ⋅∆R ⋅ 4A π ρ ⋅ R ⋅∆R ⋅d H Nanomanipulator-Beyond Moore
Use DC and AC electrokinetics to write with particles:
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Particle less polarizable than medium Nanomanipulator-Beyond Moore
Separation of Listeria from Whole Blood
Before Separation: 10 kHz, Wash blood off 10Vpp
After wash blood off Wash Listeria off Nanomanipulator-Beyond Moore
A) An array of microelectrodes is fabricated using standard photolithographic techniques
(B) nanoparticles move electrokinetically on top of a substrate and induce a submicron wide surface change. Responsive Drug Delivery Responsive Drug Delivery Responsive Drug Delivery
CaM-immobilized polymer chain
phenothiazine-immobilized polymer chain
S
Cl N
N free chlorpromazine Change in Flow Rate
Stimulus QuickTime™ and a TIFF (Uncompressed) decompressor are needed to see this picture. C-MEMS SU-8/Au(3000Å)/Ti(200Å)/SiO2/Si
before C-MEMS
Pyrolysis of patterned photoresist:
Excellent electrochemical material
Sensors
Batteries
Ultra-capacitors, etc
Mechanical/electrical properties can be selected ! C-MEMS CMOS
Battery unit
Smart switchable battery arrays: baxels are addressable just like pixels: in a serial arrangement, voltages add up; in a parallel arrangement, currents add up C-MEMS C-MEMS
Carbon film (AZ4620)
The electrolyte was 1 M LiClO4 in a 1:1 volume mixture of ethylene carbonate (EC) and dimethyl carbonate (DMC). 0.070 mAh cm-2 for the second and subsequent cycles. For a fully dense film, this corresponds to ~ 220 mAh g-1, which is within the range of reversible capacities reported for coke. Conclusions
Moore and more … The biotech century is here and wealth of nations will be more and more based on exploitation of genomics and proteomics
Molecular Diagnostics : not if but when. Merging of DNA arrays with microfluidics will enable the move from research instrument to disposable diagnostics
New less expensive detection techniques will be the other important contributor to success in molecular diagnostics Nanomanipulator to move micro- and nano-particles and even to write with those particles (non-lithography method to go beyond 0.1 µm) Move back to in-vivo because of better telemetry, batteries, sensors, MEMS and drugs. Smart pills. C-MEMS: Patterning other materials than Si. Smart , switchable batteries. Hybrid top-down and bottom-up devices. Dank u wel,
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