59 research outputs found
DC-electric-field-induced and low-frequency electromodulation second-harmonic generation spectroscopy of Si(001)-SiO interfaces
The mechanism of DC-Electric-Field-Induced Second-Harmonic (EFISH) generation
at weakly nonlinear buried Si(001)-SiO interfaces is studied experimentally
in planar Si(001)-SiO-Cr MOS structures by optical second-harmonic
generation (SHG) spectroscopy with a tunable Ti:sapphire femtosecond laser. The
spectral dependence of the EFISH contribution near the direct two-photon
transition of silicon is extracted. A systematic phenomenological model of the
EFISH phenomenon, including a detailed description of the space charge region
(SCR) at the semiconductor-dielectric interface in accumulation, depletion, and
inversion regimes, has been developed. The influence of surface quantization
effects, interface states, charge traps in the oxide layer, doping
concentration and oxide thickness on nonlocal screening of the DC-electric
field and on breaking of inversion symmetry in the SCR is considered. The model
describes EFISH generation in the SCR using a Green function formalism which
takes into account all retardation and absorption effects of the fundamental
and second harmonic (SH) waves, optical interference between field-dependent
and field-independent contributions to the SH field and multiple reflection
interference in the SiO layer. Good agreement between the phenomenological
model and our recent and new EFISH spectroscopic results is demonstrated.
Finally, low-frequency electromodulated EFISH is demonstrated as a useful
differential spectroscopic technique for studies of the Si-SiO interface in
silicon-based MOS structures.Comment: 31 pages, 14 figures, 1 table, figures are also available at
http://kali.ilc.msu.su/articles/50/efish.ht
Bridging the Pressure Gap in Water and Hydroxyl Chemistry on Metal Surfaces:  The Cu(110) Case
Computational Studies of Load-Dependent Guest Dynamics and Free Energies of Inclusion for CO 2
Ballistic Evaporation and Solvation of Helium Atoms at the Surfaces of Protic and Hydrocarbon Liquids
Atomic and molecular solutes evaporate and dissolve by traversing an atomically thin boundary separating liquid and gas. Most solutes spend only short times in this interfacial region, making them difficult to observe. Experiments that monitor the velocities of evaporating species, however, can capture their final interactions with surface solvent molecules. We find that polarizable gases such as N2 and Ar evaporate from protic and hydrocarbon liquids with Maxwell–Boltzmann speed distributions. Surprisingly, the weakly interacting helium atom emerges from these liquids at high kinetic energies, exceeding the expected energy of evaporation from salty water by 70%. This super-Maxwellian evaporation implies in reverse that He atoms preferentially dissolve when they strike the surface at high energies, as if ballistically penetrating into the solvent. The evaporation energies increase with solvent surface tension, suggesting that He atoms require extra kinetic energy to navigate increasingly tortuous paths between surface molecules
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