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High harmonic generation strongly depends on the driving laser field and as a result the harmonics have similar temporal and spatial coherence properties. [10] High harmonics are often generated with pulse durations shorter than that of the driving laser. [11] This is due to the nonlinearity of the generation process, phase matching and ...
The first nonlinear optical effect to be predicted was two-photon absorption, by Maria Goeppert Mayer for her PhD in 1931, but it remained an unexplored theoretical curiosity until 1961 and the almost simultaneous observation of two-photon absorption at Bell Labs [4] and the discovery of second-harmonic generation by Peter Franken et al. at University of Michigan, both shortly after the ...
High harmonic generation (HHG) is a nonlinear process where intense laser radiation is converted from one fixed frequency to high harmonics of that frequency by ionization and recollision of an electron. It was first observed in 1987 by McPherson et al. who successfully generated harmonic emission up to the 17th order at 248 nm in neon gas. [3]
The energy of this transition corresponds to 17th harmonic with 800 nm excitation wavelength. Similarly, in Indium, there exists a strong transition 4d 10 5s 2 → 4d 9 5s 2 5p at 19.92 eV with a high gf value of 1.11. [10] The energy of this transition corresponds to 13th harmonic with 800 nm excitation wavelength.
N-th harmonic generation. Harmonic generation (HG, also called multiple harmonic generation) is a nonlinear optical process in which photons with the same frequency interact with a nonlinear material, are "combined", and generate a new photon with times the energy of the initial photons (equivalently, times the frequency and the wavelength divided by ).
Coherent anti-Stokes Raman spectroscopy, also called Coherent anti-Stokes Raman scattering spectroscopy (CARS), is a form of spectroscopy used primarily in chemistry, physics and related fields. It is sensitive to the same vibrational signatures of molecules as seen in Raman spectroscopy , typically the nuclear vibrations of chemical bonds.
A molecular vibration is a periodic motion of the atoms of a molecule relative to each other, such that the center of mass of the molecule remains unchanged. The typical vibrational frequencies range from less than 10 13 Hz to approximately 10 14 Hz, corresponding to wavenumbers of approximately 300 to 3000 cm −1 and wavelengths of approximately 30 to 3 μm.
One of the first common applications of surface plasmon resonance spectroscopy was the measurement of the thickness (and refractive index) of adsorbed self-assembled nanofilms on gold substrates. The resonance curves shift to higher angles as the thickness of the adsorbed film increases. This example is a 'static SPR' measurement.