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3/11/2014
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1.0 Chemical Vapor Deposition(cvd)...04 2.What is CVD?.............................................................................................................05 2.1 Chemical Vapor Deposition06 2.2 Examples of CVD .......09 2.3 Generic CVD Steps 09 2.4Advantages........11 2.5 Disadvantages..11 3 Chemical Synthesis ...12 Definition for chemical synthesis.12 3.1 Nano-synthesis Technology.13 3.2 Top-down versus Bottom-up..........15 3.3Bottom-up Process - What to control ....16 3.4Colloids..........17 3.5 Colloids........18
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3.6 Nucleation & Growth.....................19 3.7Colloidal stability.....................20 3.8 Colloidal stability........................21 3.9 Methods for Nanosynthesis........................22 3.10 Sol-gel process.......................23 3.11 Advantage & Disadvantage..........................24 3.12Application.....................25
4.0 Wetdeposition techniques...........26 4.1 Self-Assembly (supramolecular approach) .28 4.1 Advantages of self-assembly...........31 4.2 Disadvantages of self-assembly..32 4.3 Applications.34 5.0 Molecular Design and modeling...43
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Chemical vapor deposition (CVD) is a widely used method for depositing thin films of a large variety of materials. Applications of CVD range from the fabrication of microelectronic devices to the deposition of protective coatings. In a typical CVD process, reactant gases (often diluted in a carrier gas) at room temperature enter the reaction chamber. The gas mixture is heated as it approaches the deposition surface, heated radiatively or placed upon a heated substrate. Depending on the process and operating conditions, the reactant gases may undergo homogeneous chemical reactions in the vapor phase before striking the surface.
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Near the surface thermal, momentum, and chemical concentration boundary layers form as the gas stream heats, slows down due to viscous drag, and the chemical composition changes.
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2.What is CVD?
Thin film formation from vapor phase reactants. Deposited films range from metals to semiconductors to insulators. An essential process step in the manufacturing of microelectronic devices. High temperatures and low pressures are the most common process conditions, but are not necessary.
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All CVD involves using an energy source to break reactant gases into reactive species for deposition.
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Molecular self-assembly is a key concept in supramolecular chemistry since assembly of the molecules is directed through noncovalent interactions (e.g., hydrogen bonding, metal coordination, hydrophobic forces, van der Waals forces, - interactions, and/or electrostatic) as well as electromagnetic interactions. Molecular self-assembly is the process by which molecules adopt a defined arrangement without guidance or management from an outside source. There are two types of self-assembly, intramolecular self-assembly and intermolecular selfassembly.
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In every case, CVD processes mustprovide 3/11/2014 a volatile precursor containing the constituents of the film transport that precursor to the deposition surface encourage or avoid reactions in the gas phase encourage surface reactions that form the film and do it rapidly, reproducibly, and uniformly for industrial applications.
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Reactants pumped through reactor. Reactants diffuse across boundary layer to surface. Reactants adsorb on surface (adatoms).
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Surface reactions; pos. formation of islands or clusters. Pos. surface diffusion of adatoms. Diffusion of by-products away from surface.
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2.4Advantages:
high growth rates possible can deposit materials which are hard to evaporate good reproducibility can grow epitaxial films
2.5 Disadvantages
high temperatures complex processes toxic and corrosive gasses
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Colloidally stable nanoparticles Reproducible Adaptable surface properties Easy + cheap (Biocompatible or biodegradable systems)
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3.4Colloids
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3.5 Colloids
To some the word `colloidal' conjures up visions of things indefinite in shape, indefinite in chemical composition and physical properties, fickle
Photographic products, ceramics, Formation of colloids for use in subsequent paper coatings, catalysts, magnetic manufacturing processes media Pumping of slurries, technology, filtration coating Handling properties of colloids, rheology, sintering
Water purification, fining of wines and Destruction of unwanted colloidal systems 20 beer
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Reactant 1 + Reactant 2
Product + By-product
Clusters
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3.7Colloidal stability
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Reactant 1 + Reactant 2
Product +
Hydrothermal methods
Microencapsulation
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3.12Application
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Snow scavenging. This is where falling snow"removes" the material below it. Nucleation scavenging. This is not a physical scavenging process strictly speaking. It stands for the conceptual representation of aerosol activation to cloud droplets within aerosol computer models. Aerosols and cloud droplets are mostly treated separately within computer models so that aerosol activation to cloud droplets represents a loss process that can be assimilated with aerosol scavenging.
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Molecular self-assembly has allowed the construction of challenging molecular topologies. An example are Borromean rings,interlocking rings wherein removal of one ring unlocks each of the other rings.
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DNA has been used to prepare a molecular analog of Borromean rings. More recently, a similar structure has been prepared using non-biological building blocks
Everyone knows how to assemble things: Just grasp the parts and put them together. Self-assembly, though, doesnt work at all like this, and as a consequence, it presents special challenges
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Improving methods for making complex structures by selfassembly is an enormously important area of research.Ive already discussed the near-term promise of nanotechnologies based on composite nanosystems that use biomolecules to organize non-biological components. Here, Id like to outline some fundamental principles will shape the role of selfassembly as nanotechnology advances.
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The architecture of biomolecular fabrication is based on the use of programmable machines to produce the complex parts necessary for self-assembly of complex systems. The same fundamental architecture can be extended to use artificial biomolecular machines (and then non-biomolecular machines), resulting in products made of better and more
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3/11/2014 Another consequence is that a self-assembled product will be partitioned by complex internal interfaces that have no operational function. Unless they are strengthened after assembly, these interfaces will weak. These are major constraints.
Mechanically directed assembly avoids these constraints. Because components need not encode the structure of a product, they can be simple and standardized, and they can be chosen for their functional properties with less concern for how they are put together This will enable more straightforward design and fabrication, but one must make the necessary machinery and I expect that this will be accomplished by means of selfassembly. 40
4.3 Applications
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Self-assembling dendrons have also been used to generate arrays of nanowires.Electron donor-acceptor complexes comprise the core of the cylindrical supramolecular assemblies, which further self-organize into two-dimensional columnar liquid crystaline lattices. Each cylindrical supramolecular assembly functions as an individual wire. High charge carrier mobilities for holes and electrons were obtained. Supramolecular assemblies are being investigated as new materials in a variety of contexts. For instance, Samuel Stupp and coworkers at Northwestern University showed that a supramolecular assembly of peptide amphiphiles in the form of nanofibers could be used to promote the growth of neurons.
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Another example with implications at the biology/materials science interface is of self-assembling dendritic dipeptides, which form hollow cylindrical supramolecular assemblies in solution and in bulk. The cylindrical assemblies possess internal helical order and self-organize into columnar liquid crystalline lattices. When inserted into vesicular membranes, the porous cylindrical assemblies mediate transport of protons across the membrane.
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One of the first requirements to initiate the molecular modeling of molecular materials is an accurate and realistic description of the electronic structure, intermolecular interactions and chemical reactions at microscopic and macroscopic scale. Therefore the first four chapters contain an extensive introduction into the latest theories of intermolecular interactions, functional density techniques, microscopic and mezoscopic modeling techniques as well as first-principle molecular dynamics
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In the following chapters, techniques bridging microscopic and mezoscopic modeling scales are presented. The authors then illustrate various successful applications of molecular design of new materials, drugs, biocatalysts, etc. before presenting challenging topics in molecular materials design.
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BY RANJITH KUMAR.R
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