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Diamond photon energy

Figure 24 Incident photon energy dependence of the surface charge separation efficiency (h" / photon) measured by PITCS. Squares, circles, triangles, and diamonds represent the results obtained for Cr-implanted rutile, Cr-doped rutile, undoped rutile, and anatase Ti02 films, respectively. Figure 24 Incident photon energy dependence of the surface charge separation efficiency (h" / photon) measured by PITCS. Squares, circles, triangles, and diamonds represent the results obtained for Cr-implanted rutile, Cr-doped rutile, undoped rutile, and anatase Ti02 films, respectively.
Lattice vacancies (missing atoms) may considerably alter the valence bonds and cause electrons to be exited by a much smaller amount of energy (such as produced by a photon of red light) that would normally be required in a perfect lattice. A diamond containing such lattice vacancies appears blue since the red components of light (the one with less photon energy) are absorbed. A minimum of one vacancy per 10 atoms is necessary for the blue color to be noticeable.l l... [Pg.266]

Table IV. Photon energies (in electron volts) for 2s ls and 2p-ls transitions for 4-MeV electrons in <110> diamond. Table IV. Photon energies (in electron volts) for 2s ls and 2p-ls transitions for 4-MeV electrons in <110> diamond.
It is well known that, following electron-hole pair generation by electron beam excitation or absorption of above-gap radiation, blue luminescence is observed in natural type lib diamond. In synthetic boron-doped diamond and boron-doped CVD diamond the luminescence may be either blue or green (61). Interpretations of the mechanisms producing these emission bands are controversial. The green luminescence shows some of the properties of donor-acceptor pan-recombination (62) but the picture is not fully consistent. Emission is expected at photon energies given by... [Pg.381]

NEA of diamond was first reported by Himpsel etal. [87]. They measured the quantum yield, that is, the total number of electrons emitted per incident photon. The onset of electron emission was observed at a photon energy of 5.5 0.05 eV,... [Pg.453]

The differences in their band structures also explain why diamond is transparent and lead is dark. Remember that substances can absorb only photons whose energies match differences between energy levels, and a colored... [Pg.726]

Temperatures as high as 2,500 K have been achieved by laser heating (LH). For such LHDAC experiments, the sample size was around 50-100 pm, the laser beam was focused to about 40 pm, and the synchrotron beam was microfocused to about 10 pm in diameter [70]. The photon-flux for the 14.4 keV ( Fe) synchrotron radiation at the focusing spot was about 10 photons s with a 1 meV energy bandwidth. This flux was reduced by a 5 mm path through diamond, via photo absorption, to 25% of its original value. For comparison the flux of the 21.5 keV radiation of Eu would be reduced to only 60%. [Pg.508]

Hudson BS and Kohler BE (1973) Polyene spectroscopy the lowest energy excited singlet state ofdiphenyloctatetraene and other linear polyenes. J Chem Phys 59 4984-5002 Hudson BS and Kohler BE (1974) Linear polyene electronic structure and spectroscopy. Ann Rev Phys Chem 25 437-460 Hudson BS and Kohler BE (1984) Electronic stmcture and spectra of finite linear polyenes. Synthetic Metals 9 241-253 Hudson BS, Ridyard JN and Diamond J (1976) Polyene spectroscopy. Photoelectron spectra of the diphenylpolyenes. J Am Chem Soc 98 1126-1129 Hudson BS, Kohler BE and Schulten K (1982) Linear polyene electronic structure and potential surfaces. In Lim EC (ed) Excited States, Vol 6, pp 1-95. Academic Press, New York Jones PF, Jones WJ and Davies B (1992) Direct observation of the 2 Ag electronic state of carotenoid molecules by consecutive two-photon absorption spectroscopy. Photochem Photohiol A Chem, 68 59-75... [Pg.157]

Apart from transistors, several other solid state devices have been discussed [78], like junctions, photon and electron beam switches and various kinds of sensors. One property of diamond which has stimulated considerable interest in the recent years is the negative electron affinity (NEA) of suitably prepared surfaces [78,80]. The electron affinity, of a material is defined as the difference between the energy of a free electron in vacuum and the bottom of the conduction band Fyac - E. In Fig. 8 the electronic bands of p-doped clean and H-terminated (111) diamond surfaces near the surface are depicted, based on the results of UV-photoemission measurements. For the H-terminated surface, the electron affinity becomes negative once an electron is injected into the conduction band from a suitable contact or by UV excitation, it will easily leave the crystal and be emitted into vacuum. This effect, which is also observed on monohydride terminated (100) surfaces, is not unique to diamond but was also observed in a few other semieonductors with high band gaps [80]. Apart from a scientific interest, the NEA of diamond makes it an attractive eandidate for the replacement of thermionic emitters as electron beam sourees and as a miniature electron emitter for field emission displays. [Pg.415]

X-ray photons can enter the cryostat and reach the Si(Li) crystal through a thin beryllium window of typically 5-10 pm thickness. The vacuum enclosure protects the detector from surface contamination and moisture condensation (at LN2 temperatures), light and scattered electrons (in electron microprobes). For measuring very low energy/long-wavelength X-rays, the beryllium window can be replaced by ultrathin diamond or aluminum coated polyimide windows or (in vacuum instruments) removed completely. [Pg.5132]


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