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CVD

In practical applications, gas-surface etching reactions are carried out in plasma reactors over the approximate pressure range 10 -1 Torr, and deposition reactions are carried out by molecular beam epitaxy (MBE) in ultrahigh vacuum (UHV below 10 Torr) or by chemical vapour deposition (CVD) in the approximate range 10 -10 Torr. These applied processes can be quite complex, and key individual reaction rate constants are needed as input for modelling and simulation studies—and ultimately for optimization—of the overall processes. [Pg.2926]

CVD gaseous reactants (precursors) delivered to a heated substrate in a flow reactor undergo tliennal reaction to deposit solid films at atmospheric or reduced pressure, and volatile side products are pumped away. CVD is used for conductors, insulators and dielectrics, elemental semiconductors and compound semiconductors and is a workliorse in tire silicon microelectronics industry. [Pg.2929]

The fundamental steps in CVD, MOCVD and MOMBE processes can be classified as follows [13] ... [Pg.2929]

It is difficult to observe tliese surface processes directly in CVD and MOCVD apparatus because tliey operate at pressures incompatible witli most teclmiques for surface analysis. Consequently, most fundamental studies have selected one or more of tliese steps for examination by molecular beam scattering, or in simplified model reactors from which samples can be transferred into UHV surface spectrometers witliout air exposure. Reference [4] describes many such studies. Additional tliemes and examples, illustrating botli progress achieved and remaining questions, are presented in section C2.18.4. [Pg.2929]

Si02, BaTiO capacitors sol—gel, sputtering, chemical vapor deposition (CVD)... [Pg.315]

Rhenium hexafluoride is used for the deposition of rhenium metal films for electronic, semiconductor, laser parts (6—8), and in chemical vapor deposition (CVD) processes which involve the reduction of ReF by hydrogen at elevated (550—750°C) temperatures and reduced (<101.3 kPa (1 atm)) pressures (9,10). [Pg.233]

Rhenium hexafluoride is a cosdy (ca 3000/kg) material and is often used as a small percentage composite with tungsten or molybdenum. The addition of rhenium to tungsten metal improves the ductility and high temperature properties of metal films or parts (11). Tungsten—rhenium alloys produced by CVD processes exhibit higher superconducting transition temperatures than those alloys produced by arc-melt processes (12). [Pg.233]

Specifications. The use of tungsten hexafluoride in CVD appHcations in the manufacture of high density siUcon chips requires a high purity product, essentially free of all metallic contaminants. Several grades of WF are available. Table 2 shows the specifications for three grades of WF. ... [Pg.258]

Silicon Epitaxy. A critical step ia IC fabricatioa is the epitaxial depositioa of sdicoa oa an iategrated circuit. Epitaxy is defined as a process whereby a thin crystalline film is grown on a crystalline substrate. Silicon epitaxy is used ia bipolar ICs to create a high resistivity layer oa a low resistivity substrate. Most epitaxial depositioas are doae either by chemical vapor depositioa (CVD) or by molecular beam epitaxy (MBE) (see Thin films). CVD is the mainstream process. [Pg.346]

CVD reactors can have one of several configurations. Each has particular advantages and disadvantages. Reactors that support wafers horizontally have difficulty controlling the deposition uniformity over all the exposed wafers. Reactors having vertical wafer support produce uniform deposition, but are mechanically complex. Barrel reactors are not suited for extended operation at temperatures greater than 1200°C. [Pg.346]

Molecular beam epitaxy is a non-CVD epitaxial process that deposits silicon through evaporation. MBE is becoming more common as commercial equipment becomes available. In essence, silicon is heated to moderate temperature by an electron beam in a high vacuum... [Pg.346]

Pa (10 10 ° Torr)) condition such that the volatile species travels at a relatively high velocity to the substrate wafer. The growth rate is 0.01-0.3 ///min which starts to be competitive with CVD deposition rates. [Pg.346]

Sihcon dioxide layers can be formed using any of several techniques, including thermal oxidation of siUcon, wet anodization, CVD, or plasma oxidation. Thermal oxidation is the dominant procedure used in IC fabrication. The oxidation process selected depends on the thickness and properties of the desired oxide layer. Thin oxides are formed in dry oxygen, whereas thick (>0.5 jim) oxide layers are formed in a water vapor atmosphere (13). [Pg.347]

Dielectric Film Deposition. Dielectric films are found in all VLSI circuits to provide insulation between conducting layers, as diffusion and ion implantation (qv) masks, for diffusion from doped oxides, to cap doped films to prevent outdiffusion, and for passivating devices as a measure of protection against external contamination, moisture, and scratches. Properties that define the nature and function of dielectric films are the dielectric constant, the process temperature, and specific fabrication characteristics such as step coverage, gap-filling capabihties, density stress, contamination, thickness uniformity, deposition rate, and moisture resistance (2). Several processes are used to deposit dielectric films including atmospheric pressure CVD (APCVD), low pressure CVD (LPCVD), or plasma-enhanced CVD (PECVD) (see Plasma technology). [Pg.347]

There are two types of deposited films known as siUcon nitride. One is deposited via plasma-enhanced CVD at temperatures <350° C (18). In this process silane and ammonia react in an argon plasma to form siUcon imide [14515-04-9] SiNH. [Pg.348]

A second type of siUcon nitride, called stoichiometric siUcon nitride, is deposited at much higher temperatures using CVD or LPCVD in the form of Si N. Stoichiometric siUcon nitride can be used as a mask for the selective oxidation of siUcon. Here the siUcon nitride is patterned over a siUcon substrate, and the exposed siUcon is oxidized. The siUcon nitride oxidizes very slowly compared to the siUcon. [Pg.348]

Metallization layers are generally deposited either by CVD or by physical vapor deposition methods such as evaporation (qv) or sputtering. In recent years sputter deposition has become the predominant technique for aluminum metallization. Energetic ions are used to bombard a target such as soHd aluminum to release atoms that subsequentiy condense on the desired substrate surface. The quaUty of the deposited layers depends on the cleanliness and efficiency of the vacuum systems used in the process. The mass deposited per unit area can be calculated using the cosine law of deposition ... [Pg.348]

Copper is an attractive metallisation element because of its high conductivity. It has been added to Al in low concentrations (AlSi(l%)—Cu(0.5%)) to improve conductive priorities. Selective, low temperature copper CVD processing, using copper(I) P-diketonate compounds, has been carried out (23). [Pg.349]

Chemical Vapor Deposition. In chemical vapor deposition (CVD), often referred to as vapor transport, the desired constituent(s) to be deposited are ia the form of a compound existing as a vapor at an appropriate temperature. This vapor decomposes with or without a reducing or oxidizing agent at the substrate— vapor interface for film growth. CVD has been used successfully for preparing garnet and ortho ferrite films (24,25). Laser-assisted CVD is also practiced. [Pg.391]


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AA-CVD

Activated CVD

Aerosol CVD

Alternative CVD Methods for Deposition of Thin ZnO Films

Applications CVD diamond

Applications of CVD Diamond

Applications of CVD Graphite

Applications of CVD Silicon

Applications of Ferroelectric CVD Materials

Atmospheric pressure CVD

BSCCO Films by CVD Using Fluorinated Metal-Organic Precursors

Beam CVD

Bias Enhanced Plasma CVD

CARBON FIBERS FROM VAPOR-PHASE (CVD) REACTION

CVD (chemical vapor

CVD - cardiovascular disease

CVD Borides for Corrosion-Resistance Applications

CVD Boron Nitride

CVD Carbides for Corrosion-Resistance Applications

CVD Ceramic Composites

CVD Cu

CVD DIAMOND PROCESSES

CVD Fabrication

CVD Ferroelectric Materials

CVD IN OPTOELECTRONICS

CVD IN POWDER APPLICATION

CVD M

CVD Metal Powders

CVD Metals for Corrosion Resistance Applications

CVD Nitrides for Corrosion-Resistant Applications

CVD Oxides for Corrosion-Resistance Applications

CVD Precursor Design Strategies for HTS Materials

CVD Processes and Equipment

CVD Production of Optical Fibers

CVD Reactions

CVD apparatus

CVD at low pressure

CVD catalyst

CVD coating

CVD diamond

CVD diamond deposition

CVD fluidized bed process

CVD growth

CVD in Cutting-Tool Applications

CVD in Electronic Applications Conductors, Insulators, and Diffusion Barriers

CVD in Electronic Applications Semiconductors

CVD in Fiber, Powder, and Monolithic Applications

CVD in Optical Applications

CVD in Wear-and Corrosion-Resistant Applications

CVD methods

CVD of BSCCO

CVD of HTS Lattice-Matched Metal Oxides

CVD of LTS Materials

CVD of Other LTS Materials

CVD of Oxides

CVD of TBCCO

CVD of TBCCO Thin Films on Single Crystal Substrates

CVD of YBCO

CVD oxide

CVD precursors

CVD process

CVD reactor

CVD silicon carbide

CVD synthesis

CVD technique

CVD tungsten source material

CVD-SiC fibers

CVD-SiO

CVD-diagrams

CVD-diamond-coated tools

CVD-prepared

CVD/PECVD

CVD—See Chemical vapor deposition

Cat-CVD

Characteristics Required for CVD ZnO Layers Incorporated within Thin Film Solar Cells

Characteristics of Plasma CVD

Chemical vapor deposition (CVD

Chemical vapour deposition, CVD

Coated Powders by CVD

Cold wall CVD

Cold-wall type CVD

Combustion CVD

Conductivity CVD diamond

Conservation of, CVD reactor

Contamination issues in CVD

Counter-diffusion CVD

DC Plasma CVD

DLC by PVD-CVD Process from a Hydrocarbon Source

Definition of CVD

Deposition CVD

Deposition in a CVD Flow Reactor

Diamond CVD Techniques

Diamond by CVD

Direct-Current Thermal Plasma CVD

Doping of CVD ZnO films

E-CVD

ECR plasma CVD

Electrochemical Characterisation of CVD Grown Graphene

Electron Cyclotron Resonance (ECR) CVD Reactor

Epitaxial CVD

Extrinsic Doping of CVD ZnO

F2 Mixtures as CVD-chamber Cleaning Gas

FB-CVD

FUNDAMENTALS OF PLASMA-ASSISTED CVD

FUNDAMENTALS OF THERMAL CVD

Film Formation from Vapor Phase by CVD

Flame CVD

Flow in a CVD Reactor

Fluidized-bed CVD

Fluorine content in CVD-WSix films

Gas flow in CVD reactors

Grades CVD diamond

Growth Mechanisms for CVD ZnO

Halide CVD of BSCCO Thin Films

High-temperature CVD

History of ZnO Growth by CVD Process

Hot filament CVD reactor

Hot-filament CVD

Hot-wall CVD reactors

Hot-wire CVD

ICP CVD

In Situ CVD Growth of BSCCO

In situ monitoring of CVD processes

Initiated CVD

Inorganic CVD

L-CVD

LA-CVD

LASER AND PHOTO CVD

Laser CVD

Laser induced CVD

Laser-assisted CVD

Laser-assisted CVD process

Laser-enhanced CVD

Laser-induced CVD Process

Low pressure CVD

MO CVD

Materials Deposited by Plasma CVD

Metal organic CVD

Metalorganic CVD

Microwave CVD

Microwave Plasma CVD Reactors

Microwave plasma CVD

Microwave plasma assisted CVD

Microwave plasma enhanced CVD

NbN CVD

NbN CVD Film Growth

NbN CVD Precursors and Reaction Schemes

Novel Plasma-Enhanced CVD Reactors

Organic CVD (MOCVD)

Oxidative CVD

PA-CVD

PE-CVD

PRODUCTION CVD REACTOR SYSTEMS

PS-CVD

PS-CVD deposition

Photo CVD

Photo enhanced CVD

Physical Properties of CVD-Derived Nb3Ge Films

Physical Properties of CVD-Derived NbN Films

Plasma CVD

Plasma CVD (PCVD)

Plasma CVD Methods

Plasma Enhanced CVD PECVD)

Plasma activated CVD

Plasma arc-jet CVD

Plasma enhanced CVD system

Plasma-CVD of Graphite

Plasma-Enhanced CVD (PECVD) Reactors

Plasma-assisted CVD

Plasma-enhanced CVD

Plasma-enhanced chemical vapor deposition PE-CVD)

Polymer CVD

Preparation Method of SAMs by CVD

Pressure Modifications in CVD

Process conditions for Chemical Vapor Deposition (CVD)

Production CVD reactors

Properties of CVD diamond

Pulsed CVD

RF thermal plasma CVD

Radio frequency plasma assisted CVD

Radio-Frequency Thermal Plasma CVD

Reaction Kinetics in CVD

Resistivity of CVD

Rotating-disk CVD reactor

Sample CVD and ALD processes

Selective CVD

Selective growth of carbon nanotube arrays synthesized by injection CVD method

SiC CVD Growth

Silicon, CVD

Sol-Gel and CVD

Some Special CVD Processes

Status of CVD Diamond Applications

Stimulated CVD

Structural Features of CVD Graphite

THE CVD OF CHROMIUM CARBIDE

THE CVD OF DIAMOND

THE CVD OF GERMANIUM

THE CVD OF GRAPHITE

THE CVD OF HAFNIUM CARBIDE

THE CVD OF NIOBIUM CARBIDE

THE CVD OF PYROLYTIC GRAPHITE

THE CVD OF REFRACTORY CARBIDES

THE CVD OF SILICON

THE CVD OF SILICON CARBIDE

THE CVD OF SUPERCONDUCTORS

THE CVD OF TITANIUM CARBIDE

THERMAL CVD OF METALLIC CONDUCTORS

THERMAL CVD of Dielectrics and Semiconductors

THERMODYNAMICS OF CVD

Technologically Significant Ceramics via CVD

The CVD Process

The CVD Process for Epi Silicon

The CVD Process for Fiber Production

The CVD of Aluminum Nitride

The CVD of Boron Carbide

The CVD of Boron Nitride

The CVD of Ceramic Materials Carbides

The CVD of Ceramic Materials Nitrides

The CVD of Ceramic Materials Oxides

The CVD of Metals

The CVD of Non-Metallic Elements

The CVD of Other Interstitial-Metal Carbides

The CVD of Silicon Nitride

The CVD of Silicon-Carbide Fibers

The CVD of Titanium Nitride

The Chemistry of CVD

The Uses of High-Sensitivity White-Light Absorption Spectroscopy in Other CVD Environments

Thermal CVD (Hot Filament)

Thermal CVD diamond

Thermal CVD reactors

Thermal laser CVD

Thermal plasma CVD

Thermal-CVD

Thermodynamic Analysis of YBCO CVD

Tin Compounds For CVD

Tin Compounds For CVD (Chemical Vapor Deposition)

Transition metal CVD precursors

Trends in CVD Optical Applications

Ultra-high vacuum CVD

Vapor Deposition (CVD) diamond

Vapour Deposition (CVD)

Wear and Corrosion Resistance Applications of CVD Coatings

YBCO CVD

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