Silicon Delta Doping in GaAs: An Ongoing Enigma

1995 ◽  
Vol 378 ◽  
Author(s):  
R. C. Newman ◽  
M. J. Ashwin ◽  
J. Wagner ◽  
M. R. Fahy ◽  
L. Hart ◽  
...  

AbstractInfrared (IR) absorption and Raman scattering are reported from the localized vibrational modes (LVM) of Al and Si δ-layer superlattices in MBE (100) GaAs grown at 400°C as a function of the total areal concentrations, [A1]A and [Si]A respectively. The Al superlattices show the expected behavior on passing from sub-monolayer (ML) to thicker layers (thin AlAs) since the impurities still occupy only Ga-sites. The behavior is very different from that found for Si δ-layers. In addition to SiGa reported previously, we now show that SiAs, SiGa-SiAs pairs and the electron trap Si-X are also present in Si δ-layers and superlattices for 0.05 ≤ [Si]A≤ 0.5 ML. The conductivity of these structures and the concentrations of substitutional Si in GaAs at all sites fall to zero for [Si]A> 0.5 ML but a Raman feature at 470–490 cm−1, attributed to the vibrations of covalent Si-Si bonds is then detected. This feature is not observed in structures containing very closely spaced dilute (0.01 ML) Si δ-planes. It is inferred that long-range Si diffusion does not occur in the bulk crystal, although there could be surface diffusion during Si deposition. The maximum measured carrier concentrations are always less than 2 × 1019 cm−3, the DX limit. The redistribution of Si amongst the various lattice sites is discussed in terms of SiGa DX-like displacements occurring during growth, followed by local thermally activated diffusion jumps. It is speculated that AsGa antisite defects and Ga-vacancies are produced by this process. The reason why the Si δ-layer is non-conducting remains unclear.

1995 ◽  
Vol 379 ◽  
Author(s):  
R. E. Pritchard ◽  
R.C. Newman ◽  
J. Wagner ◽  
M. Maier ◽  
A. Mazuelas ◽  
...  

ABSTRACTThe local environments of CAs acceptors in InxGa1−xAs and AlxGa1−xAs have been determined from the localized vibrational modes (LVMs) of both isolated CAs impurities and H-CAs pairs using infrared (IR) absorption and Raman scattering techniques. In as-grown layers of InxGa1−xAs (x<0.1), a single LVM due to isolated CAs acceptors was observed. The introduction of hydrogen led to the formation of H-CAs pairs and a single A1−-mode (stretch) and a single A1+-mode (XH) were observed for the InxGa1−xAs layers. All the LVMs were identified with carbon in CAsGa4 cluster configurations implying that less than 5 % of the detectable carbon atoms were present in clusters incorporating one or more CAs-In bonds. For AlxGa1−xAs, five stretch modes and five X-modes of the H-CAs pairs were observed for 0<x<1 and each mode was assigned to configurations for which the originally unpaired CAs had 0,1,2,3 or 4 Al nearest neighbors. These results show that carbon does not appear to form bonds with In atoms for the InxGa1−xAs samples investigated and this can explain the difficulty found in incorporating CAs acceptors in InxGa1−xAs with x>0.1 for some growth techniques. CAs acceptors can form strong bonds with both Al and Ga atoms, however, leading to a high solubility of carbon in AlxGa1-xAs over the full compositional range.


1987 ◽  
Vol 104 ◽  
Author(s):  
M. Stutzmann ◽  
C. P. Herrero

ABSTRACTWe have studied the hydrogen passivation of boron acceptors in bulk crystalline silicon with Raman scattering. Upon hydro-genation, distinct changes in the optical phonon lineshape and the localized vibrational modes of boron are observed. The hy-drogen in the passivated region gives rise to a specific Raman-active mode, whose vibrational frequency depends strongly on temperature and uniaxial stress. Implications of these results on possible structural models are discussed.


2020 ◽  
Vol 65 (6) ◽  
pp. 480
Author(s):  
N. E. Коrnienko ◽  
O. L. Pavlenko

A number of coupled Fermi vibrational resonances (FRs) in liquid benzene from a multitude of them are systematically studied. The spectral structure of the vibrational bands in the IR absorption and Raman scattering spectra are determined by their numerical decomposition into individual components. The complication of vibrational resonances with an increase in their order is due to the overlapping of FRs and the appearance of additional resonant vibrational modes. To clarify the identification of the vibrations of the benzene FR v1+v6, v8 and the correction of the frequencies of a number of inactive vibrations, including v13(E1u), the experimental results are compared to the data obtained by quantum-chemical calculations. With regard for the collective-wave properties of vibrational modes in the benzene liquid state, we propose a new content of the analysis of FRs. It should include the study of 1) the intensity changes for various spectral components in the IR absorption and Raman scattering for FR vibrational bands of various orders, 2) half-widths δv of the bands, and 3) anharmonic shifts ΔvA for various components in the vibrational bands of FRs.


2017 ◽  
Vol 8 ◽  
pp. 975-981 ◽  
Author(s):  
Alexander G Milekhin ◽  
Olga Cherkasova ◽  
Sergei A Kuznetsov ◽  
Ilya A Milekhin ◽  
Ekatherina E Rodyakina ◽  
...  

Nanoantenna-assisted plasmonic enhancement of IR absorption and Raman scattering was employed for studying the vibrational modes in organic molecules. Ultrathin cobalt phthalocyanine films (3 nm) were deposited on Au nanoantenna arrays with specified structural parameters. The deposited organic films reveal the enhancement of both Raman scattering and IR absorption vibrational modes. To extend the possibility of implementing surface-enhanced infrared absorption (SEIRA) for biological applications, the detection and analysis of the steroid hormone cortisol was demonstrated.


1971 ◽  
Vol 9 (20) ◽  
pp. 1719-1721 ◽  
Author(s):  
W. Nazarewicz ◽  
M. Balkanski ◽  
J.F. Morhange ◽  
C. Sébenne

1970 ◽  
Vol 25 (17) ◽  
pp. 1184-1187 ◽  
Author(s):  
D. T. Hon ◽  
W. L. Faust ◽  
W. G. Spitzer ◽  
P. F. Williams

2002 ◽  
Vol 13 (0) ◽  
pp. 235-238
Author(s):  
TATIANA SMIRNOVA ◽  
VAVIK TER-NERSESYANTS ◽  
MARINA PESTRIKOVA

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