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Nitrides films

Hafnium begins to react with nitrogen at about 900°C to form a surface nitride film, and reacts rapidly with hydrogen at about 700°C to form hydrides (qv). The hydrogen diffuses rapidly and converts the bulk metal into the brittle hydride. [Pg.440]

In a vacuum, uncoated molybdenum metal has an unlimited life at high temperatures. This is also tme under the vacuum-like conditions of outer space. Pure hydrogen, argon, and hehum atmospheres are completely inert to molybdenum at all temperatures, whereas water vapor, sulfur dioxide, and nitrous and nitric oxides have an oxidizing action at elevated temperatures. Molybdenum is relatively inert to carbon dioxide, ammonia, and nitrogen atmospheres up to about 1100°C a superficial nitride film may be formed at higher temperatures in the latter two gases. Hydrocarbons and carbon monoxide may carburize molybdenum at temperatures above 1100°C. [Pg.465]

Properties. Uranium metal is a dense, bright silvery, ductile, and malleable metal. Uranium is highly electropositive, resembling magnesium, and tarnishes rapidly on exposure to air. Even a poHshed surface becomes coated with a dark-colored oxide layer in a short time upon exposure to air. At elevated temperatures, uranium metal reacts with most common metals and refractories. Finely divided uranium reacts, even at room temperature, with all components of the atmosphere except the noble gases. The silvery luster of freshly cleaned uranium metal is rapidly converted first to a golden yellow, and then to a black oxide—nitride film within three to four days. Powdered uranium is usually pyrophoric, an important safety consideration in the machining of uranium parts. The corrosion characteristics of uranium have been discussed in detail (28). [Pg.319]

Early work in ellipsometry focused on improving the technique, whereas attention now emphasizes applications to materials analysis. New uses continue to be found however, ellipsometry traditionally has been used to determine film thicknesses (in the rang 1-1000 nm), as well as optical constants. " Common systems are oxide and nitride films on silicon v ers, dielectric films deposited on optical sur ces, and multilayer semiconductor strucmres. [Pg.401]

Nakamura, K., Preparation and Properties of Boron Nitride Films by Metal Organic Chemical Vapor Deposition, /. Electochem. Soc., 133-6 120-1123 (1986)... [Pg.104]

Hoffman, D. M., et al., Plasma-Enhanced CVD of Silicon Nitride Films from a Metallo-Organic Precursor, J. Mater. Res., 9(12) 3019-3021 (1994)... [Pg.104]

Poly crystalline boron nitride films, with a structure similar to rhombohedral boron carbide and a ratio of boron to nitrogen of 3 1, were produced by hot-filament CVD. This work indicates the possible existence of other boron-nitride structures. [Pg.275]

Kaplan, W., and Zhang, S., Determination of Kinetic Parameters of LPCVD Processes from Batch Depositions, Stoichiometric Silicon Nitride Films, Prac. 11th. Int. Conf. on CVD, (K. Spear and G. Cullen, eds.), pp. 381-387, Electrochem. Soc., Pennington, NJ 08534 (1990)... [Pg.291]

Monaghan, D. R, Teer, D. G., Laing, K. C., Efeoglu, I., and Ar-nell, R. D., Deposition of Graded Alloy Nitride Films by Closed Field Unbalanced Magnetron Sputtering," Surf. Coat. Technol., Vol. 5 9,1993, pp. 21 -25. [Pg.162]

McCuUoch, D. G. and Merchant, A. R., The Effect of Annealing on the Structure of Cathodic Arc Deposited Amorphous Carbon Nitride Films, Thin Solid Films, Vol. 290, 1996, pp. 99-102. [Pg.163]

Ming, Y. and Kramer, D. J., Properties of Carbon Nitride Films Deposited With and Without Electron Resonance Plasma Assistance, Thin Solid Films, Vol. 382, 2001, pp. 4-12. [Pg.164]

Wang, X., Martin, P. J., and Kinder, T. J., Optical and Mechanical Properties of Carbon Nitride Films Prepared by Ion-Assisted Arc Deposition and Magnetron Sputtering, Thin SolidFilms, o. 256, Ho. 1-2,1995,pp. 148-154. [Pg.164]

Popov, C., Zambov, L. M., Plass, M. R, and Kulisch, W., Optical, Electrical and Mechanical Properties of Nitrogen-rich Carbon Nitride Films Deposited by Inductively Coupled Plasma Chemical Vapor Deposition," Thin Solid Films, Vol. 377-378,2000, pp. 156-162. [Pg.164]

Czyzniewski, A., Precht, W., Pancielejko, M., Myslinski, P., and Walkowiak, W., Structure, Composition and Tribological Properties of Carbon Nitride Films," Thin Solid Films, Vol. 317, No. 1-2,1998, pp. 384-387. [Pg.164]

Chemical Vapor Deposition- Deposition of silicon oxide films is accomplished by CVD equipment. Either plasma CVD or ozone oxidation is used. Blanket tungsten films are also deposited by CVD equipment to create contact and via plugs. Polysilicon and silicon nitride films are deposited in hot-wall furnaces. TiN diffusion barrier films are deposited by either sputtering or CVD, the latter giving superior step coverage. [Pg.327]

Thermal nrocessing- Difiusion furnaces are used not only for the anneal of implanted dopants but for growing high quality thermcd oxides, depositing polysilicon nitride films (SiN,) and for rapid thermcd processing of deposited films. [Pg.328]

The endothermic nitride is susceptible to explosive decomposition on friction, shock or heating above 100°C [1], Explosion is violent if initiated by a detonator [2], Sensitivity toward heat and shock increases with purity. Preparative precautions have been detailed [3], and further improvements in safety procedures and handling described [4], An improved plasma pyrolysis procedure to produce poly (sulfur nitride) films has been described [5], Light crushing of a small sample of impure material (m.p. below 160°C, supposedly of relatively low sensitivity) prior to purification by sublimation led to a violent explosion [6] and a restatement of the need [4] for adequate precautions. Explosive sensitivity tests have shown it to be more sensitive to impact and friction than is lead azide, used in detonators. Spark-sensitivity is, however, relatively low [7],... [Pg.1808]

Nitride Films from Single-molecule Precursors 1040... [Pg.1006]

There have been many other reports of single-source azido precursors, all aimed at achieving device-quality films using moderate deposition conditions. The azide precursors have the advantages of (i) having preformed Ga—N bonds and (ii) only a limited number of the undesirable Ga—C and N—C bonds which can lead to carbon incorporation into the nitride films.311 A list of azido-based precursors and deposition conditions is given in Table 14. [Pg.1044]

In the case of H in low-temperature deposited silicon nitride films, ion beam techniques have again been used to calibrate IR absorption. The IR absorption cross sections most often quoted in the literature for Si—H and N—H bonds in plasma-deposited material are those of Lanford and Rand (1978) who used 15N nuclear reaction to calibrate their IR spectrometry. Later measurements in CVD nitride films, using similar techniques, confirmed these cross sections (Peercy et al., 1979). [Pg.212]

Carbon nitride, 27 214—215 conductivity of, 2 7 204-206 field emission properties of, 27 221 theoretical band structure calculations for, 27 203-204 Carbon nitride films, 2 7 205 Carbon nitride solids, 2 7 203 Carbonochloridic esters, 6 290 Carbon paper, 4 738-739 Carbon profile, in gas carburizing, 26 204 Carbon Raschig-ring tower packing, 22 745 Carbon reduction, of ferrovanadium, 25 518... [Pg.143]

A.K. Stamper and S.L. Pennington. Characterization of Plasma-Enhanced Chemical Vapor Deposited Nitride Films Used in Very Large Scale Integrated Apphcations , Journal of... [Pg.119]

The rapid developments in the microelectronics industry over the last three decades have motivated extensive studies in thin-film semiconductor materials and their implementation in electronic and optoelectronic devices. Semiconductor devices are made by depositing thin single-crystal layers of semiconductor material on the surface of single-crystal substrates. For instance, a common method of manufacturing an MOS (metal-oxide semiconductor) transistor involves the steps of forming a silicon nitride film on a central portion of a P-type silicon substrate. When the film and substrate lattice parameters differ by more than a trivial amount (1 to 2%), the mismatch can be accommodated by elastic strain in the layer as it grows. This is the basis of strained layer heteroepitaxy. [Pg.317]


See other pages where Nitrides films is mentioned: [Pg.442]    [Pg.54]    [Pg.56]    [Pg.44]    [Pg.434]    [Pg.490]    [Pg.291]    [Pg.153]    [Pg.163]    [Pg.163]    [Pg.164]    [Pg.365]    [Pg.370]    [Pg.332]    [Pg.121]    [Pg.309]    [Pg.1044]    [Pg.237]    [Pg.6]    [Pg.241]    [Pg.291]    [Pg.232]    [Pg.56]   
See also in sourсe #XX -- [ Pg.232 ]

See also in sourсe #XX -- [ Pg.161 , Pg.162 , Pg.163 , Pg.164 , Pg.165 ]




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Aluminum nitride thin films

Amorphous silicon nitride thin films

Bonded films nitriding

Boron Nitride and Carbide Films

Boron nitride thin films

Epitaxy, vapor phase nitride thin films

Germanium nitride films

Metal nitrides, thin films

Resistors, thin-film tantalum nitride

Silicon nitride and oxynitride film

Silicon nitride thin films

Titanium nitride thin films

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