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Diamond hydrogen

The structure of a-C H DLC consists of an essentially amorphous network with isolated clusters dominated by the sp configuration (graphite) with some sp (diamond). Hydrogen is believed to play an essential role in determining the bonding configuration by helping to form the sp bond, probably in a manner similar to the formation of CVD diamond. [Pg.206]

Ammonium cyanide forms colourless cubes, readily volatilized and completely dissociated at comparatively low temperatures.14 Its heat of formation from diamond, hydrogen, and nitrogen is 3-2 Cal.15 It dissolves readily in both water and alcohol, the salt being extensively dissociated in aqueous solution. It is extremely poisonous. [Pg.239]

For bulk diamond the g-value is determined to be 2.0029, which is quite close to the value of a free electron. Samples thermally freed from their surface covering show spin densities of about 7 x 10 spins per gram of material. This value decreases to as little as 2.2 x 10 spins per gram for diamond hydrogenated at... [Pg.361]

Another reason for the low background current has been suggested to be the hydrogen termination of the diamond surface, which does not contain surface carbon-oxygen functional groups. For example, the etching of as-deposited diamond (hydrogen... [Pg.562]

B1.29.6 HIGH-PRESSURE FORMS OF FAMILIAR OR USEFUL MATERIALS DIAMOND, FLUID METALLIC HYDROGEN, METALLIC OXYGEN, IONIC CARBON DIOXIDE, GALLIUM NITRIDE... [Pg.1959]

Around the same time a similar technique was iadependentiy developed whereby micrometer sized diamond crystaHites were grown (161). What is required ia esseace for the low pressure diamoad syathesis is a source of carboa (typically a hydrocarboa gas), hydrogea, and a temperature above 2000°C to convert molecular hydrogen to its atomic state. [Pg.216]

In the microwave-assisted or hot-filament-assisted CVD of diamond, methane and hydrogen gases (CH ca 1—5% and 95—99%) are used. In... [Pg.217]

At pressures of 13 GPa many carbonaceous materials decompose when heated and the carbon eventually turns into diamond. The molecular stmcture of the starting material strongly affects this process. Thus condensed aromatic molecules, such as naphthalene or anthracene, first form graphite even though diamond is the stable form. On the other hand, aUphatic substances such as camphor, paraffin wax, or polyethylene lose hydrogen and condense to diamond via soft, white, soHd intermediates with a rudimentary diamond stmcture (29). [Pg.564]

Metastable growth of diamond takes place from gases rich in carbon and hydrogen at low pressures where diamond would appear to be thermodynamically unstable. The subject has a long history, beginning with work in the United States and Russia as early as 1962 (30—32) but not achieving widespread interest and acceptance until about 1986 after successful work in Japan. [Pg.565]

In a typical use of this method, a mixture of hydrogen and methane is fed into a reaction chamber at a pressure of about 1.33 kPa (10 torr). The substrate upon which diamond forms is at about 950°C and Hes about 1 cm away from a tungsten wine at 2200°C. Small diamond crystals, 1 mm or so in si2e, nucleate and grow profusely on the substrate at a rate around 0.01 mm /h to form a dark, rough polycrystalline layer with exposed octahedral or cubic faces, depending on the substrate temperature. [Pg.565]

The presence of water vapour in the ingoing gas irrixmre has been found to suppress the formation of graphite and dins to favour diamond formation. The significant change in composition when water vapour is added, is the presence of carbon monoxide in about half the proportion of hydrogen atoms. [Pg.23]

The classification of amorphous carbon films according to carbon bond type and hydrogen content can be represented in a triangular diagram, Fig. 6 [e.g., 70]. The comers at the base of the triangle correspond to graphite (100% sp carbon) and diamond (100% sp carbon). The apex represents 100% H, but the upper limit for formation of solid films is defined by the tie line between the compositions of polyethene, -(CH2) -, and polyethyne, -(CH) -. [Pg.15]

A new, low-pressure, plasma-assisted proeess for synthesising diamonds has been found by Roy et al [83,84]. An intimate mixture of various forms of carbon with one of many metals (e.g., Au, Ag, Fe, Cu, Ni) is exposed to a microwave plasma derived from pure hydrogen at temperatures ranging from 600-1000 °C. Roy et al postulate a mechanism in which a solid solution of atomic hydrogen and the metal. Me, facilitates dissolution of carbon to form molten droplets of Me -Cj,-H. Diamonds nucleate at the surface of the droplets as the temperature is reduced. [Pg.18]


See other pages where Diamond hydrogen is mentioned: [Pg.314]    [Pg.279]    [Pg.340]    [Pg.540]    [Pg.231]    [Pg.314]    [Pg.279]    [Pg.340]    [Pg.540]    [Pg.231]    [Pg.1957]    [Pg.53]    [Pg.327]    [Pg.451]    [Pg.399]    [Pg.466]    [Pg.175]    [Pg.44]    [Pg.525]    [Pg.526]    [Pg.217]    [Pg.218]    [Pg.218]    [Pg.290]    [Pg.495]    [Pg.558]    [Pg.565]    [Pg.22]    [Pg.22]    [Pg.39]    [Pg.324]    [Pg.5]    [Pg.15]    [Pg.17]    [Pg.17]    [Pg.18]    [Pg.159]    [Pg.398]    [Pg.312]    [Pg.77]    [Pg.132]    [Pg.342]    [Pg.685]   
See also in sourсe #XX -- [ Pg.4 ]

See also in sourсe #XX -- [ Pg.4 ]




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Atomic hydrogen, diamond synthesis

Diamond hydrogen-terminated

Hydrogen atom diamond

Hydrogen reaction with diamond

Hydrogen, diamond synthesis

Hydrogen- and Oxygen-Terminated Diamond

Hydrogenation diamond

Hydrogenation diamond films

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