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Active diamond electronics

A common opinion is that diamond heteroepitaxy is a necessary step in developing active diamond electronics. This has not materialized yet, and we are waiting for innovative ideas to revolutionize the agenda. [Pg.360]

Active diamond electronics has not successfully developed. After the demonstration of rudimentary high temperature Schottky diodes and transistors, problems with the deposition of semiconductor quality thin diamond films has limited further development. Imposing step flow growth on homoepitaxial growth requires very expensive synthetic HP/HT diamond crystals cut under a specific angle. [Pg.365]

Diamond electrodes tend to be quite active for electron transfer without pretreatment, at least for some outer-sphere redox systems. Exposure to the laboratory atmosphere does not deactivate this electrode like it does other sp carbons (39). As deposited diamond... [Pg.138]

Plenary 14. A K Ramdas et al, e-mail address akr phYsics.purdue.edu (RS). Electronic RS studies of doped diamond as potential semiconducting materials. A Raman active Is (p3 2) ls (Pi/2 transition of a hole... [Pg.1218]

Electronic. Diamonds have been used as thermistors and radiation detectors, but inhomogeneities within the crystals have seriously limited these appHcations where diamond is an active device. This situation is rapidly changing with the availabiHty of mote perfect stones of controUed chemistry from modem synthesis methods. The defect stmcture also affects thermal conductivity, but cost and size are more serious limitations on the use of diamond as a heat sink material for electronic devices. [Pg.559]

A pure form of sp3 hybridized carbon is known as diamond and this may also be synthesized at the nanoscale via detonation processing. Depending on their sizes, these are classified as nanocrystalline diamond (10 nm 100 nm), ultrananocrystalline diamond (< 10 nm) and diamondoids (hydrogenated molecules, 1 nm-2 nm). Nanodiamond exhibits low electron mobility, high thermal conductivity and its transparency allows spectro-electrochemistry [20,21]. However, ultrananocrystalline diamond exhibits poor electron mobility, poor thermal conductivity and redox activity [21,22]. [Pg.74]

Diamond Ordnonce Fuze Laboratories (DOFL). A US Ordnance Corps installation located in Washington, DC. These laboratories are engaged in research development, procurement and associated activities for proximity, electronic electric fuzes and related items. This faciliry is now called Harry Diamond Laboratories... [Pg.43]

Fig. 24. Magnetic field dependence of the electronic thermal conductivity at T - 0, normalized to its value at Hc2- Circles are for LuNi2B2C, squares for UPt3 and diamonds for Nb. Note the qualitative difference between the activated thermal conductivity of the s-wave superconductor Nb and the roughly linear growth seen in UPt3, a superconductor with a line of nodes (Boaknin et al. 2001). Fig. 24. Magnetic field dependence of the electronic thermal conductivity at T - 0, normalized to its value at Hc2- Circles are for LuNi2B2C, squares for UPt3 and diamonds for Nb. Note the qualitative difference between the activated thermal conductivity of the s-wave superconductor Nb and the roughly linear growth seen in UPt3, a superconductor with a line of nodes (Boaknin et al. 2001).
It therefore seems significant that the nontransition elements of greatest solid solubility in a-Fe are A1 and Si, and this in spite of the fact that Si crystallizes in an extremely stable diamond structure because both its s and p electrons are active in bonding. [Pg.303]

The Ir film, after the BEN treatment at 920 °C for 30 min, followed by a 4-h diamond growth at 770 °C, was not covered with diamond, and there were domains of both Ir(OOl) and Ir(lll) adjacent to each other [12]. The reason for this was not clear, but both the higher stability of Ir(lll) surface over Ir(OOl), and the low activation energy of Ir atom transport seemed to contribute to this result. The formation of Ir(lll) domains after BEN and diamond growth seems to indicate that a deposition of Ir(lll) film on StTiO fOOl) will be possible not simply by electron-beam evaporation but by a post-treatment. If this is actually the case, a growth of (lll)-oriented diamond will occur on Ir(l 11). [Pg.259]

The two Fe(in) atoms are linked by two bridging oxygen atoms. This so-called diamond core may play a role in the oxygen activation chemistry of this class of enzymes. Upon two-electron reduction of the Fe(in) atoms to give two Fe(II) sites, an O2 molecule binds and bridges the Fe centres. This leads to the subsequent formation of various intermediates, generally denoted compovmds O, P... [Pg.201]


See other pages where Active diamond electronics is mentioned: [Pg.3233]    [Pg.414]    [Pg.138]    [Pg.139]    [Pg.139]    [Pg.2806]    [Pg.180]    [Pg.50]    [Pg.81]    [Pg.346]    [Pg.583]    [Pg.191]    [Pg.82]    [Pg.242]    [Pg.58]    [Pg.713]    [Pg.484]    [Pg.42]    [Pg.219]    [Pg.4]    [Pg.369]    [Pg.105]    [Pg.74]    [Pg.126]    [Pg.73]    [Pg.202]    [Pg.334]    [Pg.36]    [Pg.571]    [Pg.1130]    [Pg.423]    [Pg.157]    [Pg.419]    [Pg.329]    [Pg.331]    [Pg.202]   
See also in sourсe #XX -- [ Pg.365 ]




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