Document 7230105

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Transcript Document 7230105

FILMS - FORM?

Supported - substrate type and effect of interface

Free standing - synthetic strategy

Epitaxial - lattice matching - tolerance

Superlattice - artificial

Patterned - chemical or physical lithography – bottom or top-down methods

FILMS - WHEN IS A FILM THICK OR THIN?

Monolayer - atomic, molecular thickness

Multilayer - compositional superlattice - scale - periodicity

Bulk properties - scale - thickness greater than

l(

e,h)

Quantum size effect - 2D spatial confinement – quantum confined along z, free electron behavior along x,y – called quantum wells – enable quantum devices

THIN FILMS VITAL IN MODERN TECHNOLOGY

Protective coatings

Optical coatings, antireflection coatings

Electrochromic windows

Dielectric film – low k circuit packaging – high k gate insulation

Filters, mirrors, lenses

Microelectronic devices

Optoelectronic devices

Photonic devices

THIN FILMS VITAL IN MODERN TECHNOLOGY

Electrode surfaces

Photoelectric devices, photovoltaics, solar, fuel cells

Xerography, photography

Electrophoretic, electrochromic intelligent inks, displays

Catalyst surfaces

Information storage - magnetic, magneto resistant, magneto-optical, optical, flash, nano indentation Millepede memories

FILM PROPERTIES - ELECTRICAL, OPTICAL, MAGNETIC, MECHANICAL, ADSORPTION, PERMEABILTY, CHEMICAL

• • • • • •

Thickness and Surface : Volume ratio Surface vs bulk structure - surface reconstruction, dangling bonds – unsatisfied valencies, surface roughness Hydrophobicity - hydrophilicy - wettability Composition Texture - single crystal, microcrystalline, orientation Form - supported or unsupported (free-standing) nature of substrate - patterned or un-patterned

METHODS OF SYNTHESIZING THIN FILMS

ELECTROCHEMICAL, PHYSICAL, CHEMICAL

Cathodic or anodic

Electroless deposition

Laser ablation

Cathode sputtering, vacuum evaporation, e-gun

Thermal oxidation, nitridation

METHODS OF SYNTHESIZING THIN FILMS

ELECTROCHEMICAL, PHYSICAL, CHEMICAL

Liquid phase epitaxy

Self-assembly, surface molecule anchoring, monolayers or multilayers

Discharge (plasma) techniques - RF, microwave

Chemical vapor deposition CVD, metal organic chemical vapor deposition MOCVD

Molecular beam epitaxy, supersonic cluster beams, aerosol deposition

ANODIC OXIDATIVE DEPOSITION OF FILMS

Deposition of oxide films, such as alumina, titania by oxidation of metal electrode in aqueous salts or acids

Deposition of conducting polymer films by oxidative polymerization of monomer , such as thiophene, pyrrole, aniline, acetylene

ANODIC OXIDATION OF Al IN OXALIC OR PHOSPHORIC ACID TO FORM ALUMINUM OXIDE

Pt|H

3

PO

4

, H

2

O|Al

Al

Al 3+

+

3e -

ECCell Anode

PO 4 3 -

+2e

-

PO

3 3-

+

O 2-

Cathode

2Al 3+ + 3O 2-

 g

-Al

2

O

3

(annealing)

 a

-Al 2 O 3

Voltage control of oxide thickness

Al

3+

/O

2-

diffuse through growing layer of Al

2

O

3

ANODIC OXIDATION OF PATTERNED Al DISC TO MAKE PERIODIC NANOPOROUS Al 2 O 3 MEMBRANE How to remove residual Al and Al 2 O 3 barrier layer???

2Al + 3PO 4 3-

Al 2 O 3 + 3PO 3 3 2Al + 3C 2 O 4 2-

Al 2 O 3 + 6 CO + 3O 2-

ANODIC OXIDATION OF PATTERNED Al DISC TO MAKE PERIODIC NANOPOROUS Al 2 O 3 MEMBRANE

Aqueous HgCl 2 dissolves Al to give Hg and Al(H 2 O) 6 3+ and H 3 PO 4 Al(H 2 O) 6 3+ dissolves Al 2 O 3 barrier layer to give - yields open channel membrane

ANODIC OXIDATION OF LITHOGRAPHIC PATTERNED Al TO PERIODIC NANOPOROUS Al 2 O 3

Not bad for chemistry!!!

ANODIC OXIDATION OF LITHOGRAPHIC PATTERNED Al TO PERIODIC NANOPOROUS Al 2 O 3 40V

Voltage control of channel diameter 50-500 nm accessible

60V 80V

PROPOSED MECHANISM OF ALUMINA PORE FORMATION IN ANODICALLY OXIDIZED ALUMINUM SELF ORGANIZED SELF LIMITING GROWTH OF PORES Electric and strain fields guide and organize hcp channel growth

Templated synthesis of metal barcoded nanorods

Collection of multi-metal nanorods imaged in optical microscopy by the different reflectivity’s of different metals, Science 2001, 294, 137

Optical (A) and FE-SEM (B) images of an Au-Ag multi-stripe nanorods

550-nm Au stripes and Ag stripes of 240, 170, 110, and 60 nm -top to bottom 240 nm 550 nm 170 nm 110 nm 60 nm

Orthogonal assembly on nanorods. Butyl isonitrile is bound to Pt and Au surfaces. Aminoethanethiol displaces isonitriles on gold but not on platinum. Rhodamine isocyanate is reacted with terminal amino groups to fluorescently label gold segments.

-NH-CS-NH-

thiourea linkage of rhodamine fluorescent dye to Au segment

DNA sandwich hybridization assay on metal barcode nanorods - Science 2001, 294, 137

SYNTHESIS OF CHEMICALLY POWERED NANOROD MOTORS ?

ANODIC OXIDATION OF Si TO FORM POROUS Si: THROWING SOME LIGHT ON SILICON

Typical electrochemical cell to prepare PS by anodic oxidation of heavily doped p + type Si

PS comprised of interconnected nc-Si with H/O/F surface passivation

nc-Si right size for QSEs and red light emission observed during anodic oxidation – electroluminescence

ELECTRONIC BAND STRUCTURE OF DIAMOND SILICON LATTICE

• • • • • •

band structure of Si computed using density functional theory with local density and pseudo-potential approximation diamond lattice, sp 3 bonded Si sites VB maximum at k = 0, the

G

point in the Brillouin zone, CB minimum at distinct k value indirect band gap character, very weakly emissive behavior absorption-emission phonon assisted photon-electron-phonon three particle collision very low probability, thus band gap emission efficiency low, 10 -5 %

SEMICONDUCTOR BAND STRUCTURE: CHALLENGE, EVOKING LIGHT EMISSION FROM Si

• •

EMA R exciton ~ 0.529

e

/m o mass of exciton m o = m e m where h /(m e

e

= dielectric constant, reduced + m h ) Note exciton size within the bulk material defines the size regime below which significant QSEs on band structure are expected to occur, clearly < 5 nm to make Si work

REGULAR OR RANDOM NANNSCALE CHANNELS IN ANODICALLY OXIDIZED SILICON WAFERS

Anodized forms of p + type Si wafer

Showing formation of random (left) and regular (right) patterns of pores

Lithographic pre texturing directs periodic pore formation

PORE FORMING PROCESS IN ANODICALLY OXIDIZED SILICON WAFERS

Basics of electrochemical cell - p + -Si wafer anode in contact with aqueous HF electrolyte

Mechanism of natural self limiting process for regular pore formation based on wider band gap of PS compared to bulk Si and respective redox potentials for anodic oxidation

KEY ISSUES: ORIGIN OF PHOTO- AND ELECTROLUMINESCENE OF POROUS SILICON

• • • • • •

Origin of luminescence key point- as bulk Si is indirect band gap semiconductor with very weak light emission Models for light emission include quantum spatial confinement, siloxenes, and SiOH Luminescent nc-Si structure requires SiO, SiH surface bonds - caps dangling bonds removes killer traps in band gap Size dependence of k,

m

selection rules, scaling laws determine light emission properties Mechanical, photochemical, chemical stability are key factors for devices Efficient e-h charge-injection required for practical LED

MAKING NANOCRYSTALLINE SILICON LUMINESCENT: CAPPING CB VB CB VB

*(SiH ) capping Si cluster dangling bond with H, F, O forms bonding-antibonding

orbitals, moves killer trap states out of the gap facilitates radiative relaxation

(SiH) Si n H x Si n

LIGHT WORK BY THE SILICON SAMURAI: WHERE IT ALL BEGAN AND WHERE IT IS ALL GOING FROM CANHAM’S 1990 DISCOVERY OF PL AND EL ANODICALLY OXIDIZED p-DOPED Si WAFERS, TO NEW LIGHT EMITTING SILICON NANOSTRUCTURES, TO SILICON OPTOELECTRONICS, TO PHOTONIC COMPUTING

CHEMICAL VAPOUR DEPOSITION

• • • • • •

Pyrolysis, photolysis, chemical reaction, discharges RF, microwave facilitated deposition processes Epitaxial films, correct matching to substrate lattice CH 4 + H 2 (RadioF, MicroW)

C, diamond films (perfect non-stick frying pan – inert, hard, transparent, non-stick, high thermal conductivity) Et 4 Si (thermal, air)

SiO 2 SiCl 4 or SiH 4 (thermal T, H 2 )

a-H:Si or nc-H:Si SiH 4 + PH 3 (RF)

n-Si (ppm P)

CHEMICAL VAPOUR DEPOSITION

Si 2 H 6 + B 2 H 6 (RF)

p-Si (ppm B)

Single source precursor SiH 3 SiH 2 SiH 2 PH 2 (RF)

n-Si

Me 3 Ga (laser photolysis, heating)

Ga

Me 3 Ga + AsH 3 + H 2 (T,P)

GaAs + CH 4

Si (laser evaporation, molecular beam, high to low P supersonic jet, ionization) Si n + deposition)

Si (size selected MS - cluster

H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H Amorphous hydrogenated silicon a-H:Si, easy to form thin film by CVD Hydrogen capping of dangling surface sp3 bonds Reduces surface electron killer traps Enhances electrical conductivity compared to a-Si but less than bulk c-Si Poly-domain texture Useful for pn and pin junction solar cell large area devices

REMOVING DANGLING BONDS BY Si-H CAPPING CB VB CB VB

*(SiH ) capping Si cluster dangling bond with H, F, O forms bonding-antibonding

orbitals, moves killer trap states out of the gap facilitates charge transport and radiative relaxation

(SiH) Si n H x Si n

METAL ORGANIC CHEMICAL VAPOR DEPOSITION, MOCVD

Invented by Mansevit in 1968

Recognized high volatility of metal organic compounds as sources for semiconductor thin film preparations

Enabling chemistry: electronic, optical quantum devices

Quantum wells and superlattices

Occurs for 5-500 Angstrom layers

Known as artificial superlattices

Schematic energy band diagram of a quantum well structure showing confined electron and hole states produced by large Eg GaAlAs layers sandwiching small Eg GaAs depicting quantization effects and some possible optical transitions

CB edge GaAlAs CB/VB edges GaAs L

E n = n 2

p

2 h 2 /2m*L 2

VB edge GaAlAs

METAL ORGANIC CHEMICAL VAPOR DEPOSITION, MOCVD

Quantum confined electrons and holes when thickness of quantum well L is comparable to the wavelength of an electron or hole at the Fermi level of the material, band diagram shows confined particle states and quantization effects for electrical and optical properties

Discrete electronic energy states rather than continuous bands, given by solution to the simple particle in a box equation, assuming infinite barriers for the wells, m* is the effective mass of electrons and holes

E n = n 2

p

2 h 2 /2m*L 2

Tunable thickness, tailored composition materials,

do it yourself quantum mechanics materials for the semiconductor industry

METAL ORGANIC CHEMICAL VAPOR DEPOSITION,

MOCVD

Quantum well structure synthesized by depositing a controlled thickness superlattice of a narrow band gap GaAs layer sandwiched by two wide band gap Ga x Al 1-x As layers using MOCVD

Ga(Al)Me 3 + AsH 3 (

H

2 , T)

Ga(Al)As +

CH

4

Artificial superlattices, designer periodicity of layers, quantum confined lattices, thin layers, epitaxially grown, x determines electronic band gap

Example: Ga

x

Al

1-x

As|GaAs|Ga

x

Al

1-x

As

MOCVD

• •

Example: Ga x Al 1-x As|GaAs|Ga x Al 1-x As n- and p-doping achievable by having excess As or Ga respectively in a GaAs layer

• •

Composition and carrier concentration controls refractive index (cladding, TIR optical confinement) and electrical conductivity (p-n and p-n-p junction devices), in a semiconducting superlattice Enables electron (quantum) and photon (RI) confinement for electronic and optoelectronic and optical devices

Multiple quantum well laser, quantum cascade laser, distributed feedback laser, resonant tunneling transistor, high electron mobility ballistic transistor (HEMT), laser diode

Resonant tunneling transistor

BAND GAP ENGINEERING OF SEMICONDUCTORS

MOCVD, LPE, CVD, CVT, MBE all deposition techniques that provide angstrom precise control of film thickness

Together with composition control one has a beautiful synthetic method for fine tuning the electronic band gap and hence most of the important properties of a semiconductor quantized film

BAND GAP ENGINEERING OF SEMICONDUCTORS

Key is to achieve

epitaxial lattice matching

of film with underlying substrate

Avoids interfacial lattice strain, elastic deformation, misfit dislocations, defects all of these problems serve to increase carrier scattering, decrease charge-transport, increased quenching of e-h recombination luminescence (killer traps), thereby reducing the efficacy of the material for advanced device applications

MOCVD SINGLE SOURCE PRECURSORS

• • •

Me 3 Ga, Me 3 Al, Et 3 In (synthesis GaCl 3 + MeLi/R 2 Mg/RMgI)

• • • • •

NH 3 , PH 3 , AsH 3 (synthesis Mg 3 As 2 /HCl) H 2 S, H 2 Se Me 2 Te, Me 2 Hg, Me 2 Zn, Me 4 Pb, Et 2 Cd E.g. synthesize an IR detector based on p-n photodiode Me 2 Cd + Me 2 Hg + Me 2 Te (H 2 , 500 o C)

Cd x Hg 1-x Te

p-Hg

x

Cd

1-x

Te/n-Hg

x

Cd

1-x

Te

p- and n-doping requires precise control of Hg/Cd and Te stoichiometry x determines the electronic bandgap – tuned to IR wavelength range for detector

Toxic materials – safe handling and disposal of toxic waste!!!

Schematic of cold wall MOCVD system

Single crystal substrate on inductively heated or resistively heated susceptor – mass flow control of precursors

MOCVD deposited film

Water cooling Thermocouple Waste gases H 2 /AsH 3 /PH 3 H 2 /InMe 3 /GaMe 3 H 2 /PEt 3 H 2 /n-dope H 2 S/p-dope ZnMe 2

MOCVD surface chemistry of precursors, nucleation and growth of product film on substrate CH 4 Me Me Ga Me Me Me Me Ga H Me Me Al Me H H As H As Al As Al As Al As Al As Al As Al As Al As Al As Al As

Precursor adsorption on single crystal oriented substrate

- lattice matching epitaxy criteria - surface physisorption - chemisorption surface diffusion - dissociative chemisorption - reaction - desorption Different models for film nucleation and growth - depends whether surface diffusion involved - fixed vs mobile crystal nuclei

MOCVD SINGLE SOURCE PRECURSORS

Specially designed MOCVD reactors, hot and cold wall designs, controlled flow of precursors using digital mass flow meters directing precursors to heated single crystal substrate, induction or resistive heater, silicon carbide coated graphite susceptor for mounting substrate

This chemistry creates problems for semiconductor manufacturers wrt safe handling and disposal of toxic waste

Most reactions occur in range 400-1300 o C,

complications of diffusion at interfaces

, disruption of atomically flat epitaxial surfaces/interfaces may occur during deposition

Photolytic processes (

photoepitaxy

more reasonable temperatures ) help to bring the deposition temperatures to

PHOTOEPITAXY

Making atomically perfect thin films under milder and more controlled conditions

Et 2 Te + Hg + H 2 (h

, 200 o C)

HgTe + 2C 2 H 6

Bottom graphite, middle substrate, top HgTe film H 2 gas window Exhaust gases UV illumination Hg pool H 2 /Et 2 Te

PHOTOEPITAXY

Making atomically perfect thin films under milder and more controlled conditions

Mullin and Tunnicliffe 1984

Et 2 Te + Hg (pool) + H 2 (

h

, 200 o C

)

HgTe + 2C 2 H 6

Et 2 Te/Me 2 Cd + Hg (pool) + H 2 2C 2 H 6 (

h

, 200 o C

)

Hg x Cd 1-x Te +

MOCVD preparation requires 500 o C using Me 2 Te + Me 2 Hg/Me 2 Cd

Advantages of photo-epitaxy

Lower temperature operation,

multi-layer formation, less damage of layers

- ternaries Hg quantum size effect devices Hg x x Cd Cd 1-x and Hg/Cd rich, p-n diodes, IR photodetectors, multi-layers, 1-x Te, n- and p-doping, Te Te|HgTe|Hg x Cd 1-x Te

PHOTOEPITAXY

Making atomically perfect thin films under milder and more controlled conditions

Lower interlayer diffusion, easy to fabricate

Abrupt boundaries, less defects, strain and irregularities at interfaces

Note that H 2 gas window in apparatus prevents deposition of HgTe on observation port

In this way CdTe can be deposited onto GaAs at 200 250 o C even with a 14% lattice mismatch

Key consideration - GaAs is susceptible to damage under MOCVD conditions 650-750 o C

REQUIREMENTS OF SUCCESSFUL MOCVD PRECURSOR

RT stable

No polymerization, decomposition

Easy handling

Simple storage

Not too reactive

Vaporization without decomposition

REQUIREMENTS OF MOCVD PRECURSORS

Vaporization without decomposition

Modest < 100 o C temperatures

Low rate of homogeneous pyrolysis, gas phase, wrt heterogeneous, surface, decomposition

HOMO : HETERO rates ~ 1 : 1000

Heterogeneous reaction preferred on substrate

Greater than on other hot surfaces in reactor

REQUIREMENTS OF MOCVD PRECURSORS

Not on supports or reaction chamber/vessel

Ready chemisorption of precursor on substrate

Detailed surface and gas phase studies of structure of adsorbed species, reactive intermediates, kinetics, vital for quantifying film nucleation and growth processes

Electrical, magnetic, optical films made in this way

Semiconductors, metals, silicides, nitrides, oxides, mixed oxides (e.g., high Tc superconductors)

CRITICAL PARAMETERS IN MATERIALS PREPARATION FOR SYNTHESIS OF THIN FILMS

Composition control - precise command over stoichiometry and adventitious carbonaceous deposits

Variety of materials to be deposited

Good film uniformity

Large areas to be covered, > 100 cm 2

Precise reproducibility

CRITICAL PARAMETERS IN MATERIALS PREPARATION FOR SYNTHESIS OF THIN FILMS

Growth rate, thickness control

2-2000 nm layer thickness

Precise control of film thickness

Accurate control of deposition, film growth rate

CRITICAL PARAMETERS IN MATERIALS PREPARATION FOR SYNTHESIS OF THIN FILMS

Crystal quality, epitaxy

High degree of film perfection

Defects degrade device performance

Reduces useable wafer yields

CRITICAL PARAMETERS IN MATERIALS PREPARATION FOR SYNTHESIS OF THIN FILMS

Purity of precursors

Usually less than 10

-9

impurity levels

Stringent demands on starting material purity

Chemistry challenge, purifying, analyzing precursors at ppb level

Demands exceptionally clean growth system otherwise defeats the object of controlled doping of films for device applications

CRITICAL PARAMETERS IN MATERIALS PREPARATION FOR SYNTHESIS OF THIN FILMS

Interface widths

Abrupt changes of composition, dopant concentration required, vital for quantum confined structures

30-40 sequential layers often needed

Alternating composition and graded composition films

0.5-50 nm thickness required with atomic level precision

All of the above has been more-or-less perfected in the electronics and optics industries – amazing achievement!!!

III-V BAND GAP ENGINEERING

• • • • • • • • • • • •

Designer semiconductors

Single crystal substrate Single crystal layers

Zinc blende lattice Lattice constant Composition Doping Thickness Multilayers Epitaxial lattice matching Control of Eg band gap and RI refractive index Operating wavelengths for optical telecommunication systems labeled in purple

TECHNIQUES USED TO GROW SEMICONDUCTOR FILMS AND MULTILAYERED FILMS

• •

MOCVD

Liquid phase epitaxy

Chemical vapor transport

Molecular beam epitaxy

• •

Laser ablation Used for band gap engineering of semiconductor materials that function at 1.5 microns in near IR integrating with glass fiber optics and waveguides

6InP/3GaAs/6InP EPITAXIALLY MATCHED SUPERLATTICE

TAILORED BAND GAPS - DESIGNER MOCVD

GRADED COMPOSITION

POTENTIAL WELLS Al x Ga 1-x As graded composition-gap superlattice e CB AlAs wide gap Tunable h

h CB GaAs narrow gap VB GaAs narrow gap VB AlAs wide gap Designer quantum well architecture band gap engineering - graded composition enables gradient potential – speeds mobility of electrons injected into channel used to enhance performance in high electron mobility transistors HEMTs or build a quantum cascade laser

Federico Capasso co-inventor of the quantum cascade laser imagined small things when he used size and dimensionality of materials to tailor their properties for electronic and optical devices

h

h

h

QUANTUM CASCADE LASER A NICE EXAMPLE OF BAND GAP ENGINEERING BY MOCVD

White bands in the TEM are QWs made of

narrow band gap GaInAs

, which are sandwiched between barrier layers of

wide band gap AlInAs

ranging in thickness from atomic to 12 atomic layers

All wells are part of a QCL

Voltage applied to device, electrons move down potential barrier from wide to narrow Eg QWs and emit a photon between two thickest QWs

.

Electrons move on to the next stage to the right where the process repeats – hence cascade laser.