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Physical vapour deposition

Physical vapour deposition (PVD) is a variety of vacuum deposition and is a general term used to describe any of a variety of methods to deposit thin fdms by the condensation of a vapourized form of the desired film material on to various workpiece surfaces (e.g., on to semiconductor wafers). The coating method involves purely physical processes such as high temperature vacuum evaporation with subsequent condensation, or plasma sputter bombardment rather than involving a chemical reaction at the surface to be coated as in chemical vapour deposition. [Pg.186]

Pin on disc tester Wear and friction coefficient test [Pg.186]

Nanoindentation Hardness test for thin-fihn coatings [Pg.186]

Synthesis of intermetallics can be performed from their constituents involving the gas phase by using various methods. Notice that the presence of the gas phase may be relevant in several kinds of synthesis. A special role, however, is played by the gas phase in some groups of interrelated methods, which are generally defined as physical vapour deposition, chemical vapour deposition, vapour phase transport. [Pg.582]

It corresponds to the condensation of a gaseous species onto a suitable substrate. In this process, the molten metal is evaporated from single or multiple bath co-deposition and allowed to condense on a substrate (possibly a rotating collector). Heat sources which have been used include electron-beam and induction techniques. [Pg.582]

Preparation ofAl2S3 Aluminium and sulphur react slowly even at 800°C because liquid Al becomes coated with a skin of sulphide which acts as a barrier to further reaction. With the addition of I2 and a temperature gradient of 100°C, the aluminium sulphide separates as large colourless crystals at the cool end (700°C) of the reaction tube. This is because the transport of AI2S3 occurs via the following reactions and the formation of gaseous A1I3  [Pg.583]

Preparation ofNb5Si3 Metallic niobium and silicon dioxide do not react if heated (for instance at 1100°C) under vacuum. In the presence of traces of H2 or I2 the formation of transporting compounds (SiO or Nbl4) is observed, followed by their migration and reaction according to the following schemes  [Pg.583]


As noted above, amorphous carbon films can be produced from carbon-containing gas phases (physical vapour deposition, PVD). They can also be produced from hydrocarbon-containing gases (chemical vapour deposition, CVD), Both PVD and CVD processes can be thermally-activated or can be plasma- and/or electric field-assisted processes (e.g., microwave assisted CVD and ion beam deposition). As a consequence a wide range of processes have been developed to form amorphous carbon films and a correspondingly complex nomenclature has evolved [70, 71],... [Pg.35]

Carbides and nitrides can be prepared in many ways (chemical vapour deposition, physical vapour deposition, precipitation of salts containing metal, carbon and oxygen followed by reduction and annealing, reaction of a metal or its oxides with a gas or with solid carbon). Carbides and nitrides are often nonstoichiometric with complex phase diagrams.4-9 The compounds sometimes contain multiple phases and impurities, notably oxygen. This can lead to even more complex compounds, like oxycarbides, carbonitrides or oxycarbonitrides. [Pg.150]

There are two ways in which coatings can be applied thermomechanical processes (e.g. detonation gun, flame spraying and plasma spraying) and vapour phase deposition processes. The latter category can be subdivided into CVD (chemical vapour deposition) and PVD (physical vapour deposition). In the case of a CVD process, a chemical reaction takes place in an oven and as a result the coating material is formed and deposited on the object. Figures 11.7.9 and 11.7.10 are representations of two methods to apply coatings. [Pg.294]

Physical Vapour Deposition (PVD) is another coating technique. The reactants (precursors) are solids, which are forced in a gaseous state. This can be done by simple heating, but mostly, this procedure involves ion - bombing in order to create a plasma. The gaseous phase deposits on the solid substrate at relatively low temperatures. [Pg.449]

High Physical Vapour Deposition (PVD) (coating of various... [Pg.2]

A large amount of systematic development work on new high-performance mixed carbide, nitride, boride and oxide coating materials produced by physical vapour deposition (PVD) techniques is being carried out, because the mixed coatings often display significantly improved properties (e.g. wear-, corrosion-, oxidation-resistance or certain physical property behaviour) compared to the properties of the individual constituents. [Pg.197]

Whilst the above definition introduces the basic high level understanding and observations of the process, a more concise and scientific definition for CVD is a process whereby a thin solid film is deposited onto a substrate through chemical reactions of the gaseous species. For structural component applications, the deposition typically takes place at a temperature of around 1000°C. It is the reactive processes that distinguish CVD process from physical vapour deposition (PVD) processes, such as physical evaporation process, sputtering and sublimation processes [1],... [Pg.1]

Thin-film formation is described as a sequential process which includes nucleation, coalescence and subsequent thickness growth, whereby all states can be influenced by deposition parameters, such as temperature, pressure, gas flow rate, etc. [3,4], For physical vapour deposition (PVD) processes, significant works have been published and progess made in understanding the microstructure evolution of the films. In the atomistics of growth processes, there exists much in common bewteen CVD and PVD. Theories from PVD processes can thus be used to analyse the microstructure evolution of CVD processes [5, 6],... [Pg.216]

CVD is to be distinguished from physical vapour deposition (PVD), which also produces a thin film on a surface from the gaseous phase but without any chemical reaction. A simple illustration of PVD is the conversion of water into ice flakes and its deposition on a cold surface as snow. It starts off as H20 and finishes as H20, albeit in a different form. [Pg.349]

Various techniques are currently available for the manufacture of FGMs, in particular the chemical and physical vapour deposition methods . However, using these methods, it is very difficult to produce FGMs of the greater thickness widely required in manufacturing industry. [Pg.344]

In electrical engineering, they have utilisation potential in feeler sensors, resisters, magnetic shields, lossless optical fibres and superconductors. Methods of manufacture vary, but include the chemical and physical vapour deposition methods, the electrolytic deposition method, the atomised metal spray method, and a method in which powdered material is first melted in a plasma jet and then deposited... [Pg.374]

DCNDBQT was physically vapour deposited (PVD) under ultra high vacuum conditions (UHV) with a pressure of 5 x 10 mbar. The substrates (TiOj/Si) were annealed to 180 °C for 20 minutes in order to remove any water layer from the surface. The molecules were evaporated from homebuilt boron nitride crucibles at an evaporation rate of 1.0-1.5 ml min with the substrates kept at room temperature. The deposition rate was monitored with a quartz microbalance and a frequency counter. [Pg.683]

Electron beam physical vapour deposition (EBPVD) uses a target anode that is bombarded with an electron beam generated by a charged tungsten filament under high vacuum (Figure 5.16). [Pg.163]

PLD is a thin film deposition technique akin to physical vapour deposition (PVD) whereby a high-power pulsed laser beam is focused inside a vacuum chamber to strike a target of the material to be deposited (Figure 5.47). [Pg.219]


See other pages where Physical vapour deposition is mentioned: [Pg.301]    [Pg.919]    [Pg.707]    [Pg.582]    [Pg.583]    [Pg.595]    [Pg.46]    [Pg.47]    [Pg.127]    [Pg.57]    [Pg.437]    [Pg.449]    [Pg.450]    [Pg.571]    [Pg.571]    [Pg.113]    [Pg.1]    [Pg.149]    [Pg.163]    [Pg.166]    [Pg.170]    [Pg.3]    [Pg.518]    [Pg.632]    [Pg.718]    [Pg.485]   
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