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Mark J Abel

Publications and source records attributed to Mark J Abel.

4 recordsLinked to original sources

Heterodyne mixing of laser fields for temporal gating of high-order harmonic generation.

The concept of heterodyne mixing of laser fields is theoretically applied to the process of high-harmonic generation to enhance and modulate the kinetic energy of the active electron on subcycle time scales. A very small amount of intensity in the heterodyne field creates a significant modification of the electron kinetic energy, due to its amplification by the strong fundamental field in the kinetic-energy term, in which the heterodyne mixing occurs. Quantum calculations are carried out to verify the predictions of the classical results, demonstrating very good qualitative and quantitative agreement. Applications of the heterodyne-mixing concept are the extension of the harmonic cutoff to higher photon energies and the temporal gating of attosecond pulse production.

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Circular phase mask for control and stabilization of single optical filaments.

We experimentally demonstrate an efficient way to control and stabilize single optical filaments initiated by ultrashort laser pulses in a rare gas medium. This is done by the application of a stationary two-dimensional phase mask to the laser beam prior to focusing. Simple circular phase-step patterns of a given radius and relative phase are sufficient to stabilize the pointing of the filament output and to optimize the spectral bandwidth of the light without any resulting loss of input laser power.

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Single attosecond pulse generation in the multicycle-driver regime by adding a weak second-harmonic field.

We present a method of producing single attosecond pulses by high-harmonic generation with multicycle driver laser pulses. This can be achieved by tailoring the driving pulse so that attosecond pulses are produced only every full cycle of the oscillating laser field rather than every half-cycle. It is shown by classical and quantum-mechanical model calculations that even a minor addition (1%) of phase-locked second-harmonic light to the 800 nm fundamental driver pulse for high-harmonic generation leads to a major (15%) difference in the maximum kinetic energies of the recombining electrons in adjacent half-cycles.

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Coherent Raman spectra of the nu1 mode of carbon suboxide.

High-resolution (0.001 cm(-1)) coherent anti-Stokes Raman spectroscopy (CARS) has been used to study the nu1 symmetric CO stretching mode of the quasi-linear molecule carbon suboxide, C3O2. Q-branch transitions are seen that originate from the ground state and from thermally populated levels of the nu7 CCC bending mode, which is of unusually low frequency. The intensity variation of the Q-branch features on cooling to about 120 K in a jet expansion requires the reversal of the order of assignment given in a previous Raman study at low resolution. The identification of the nu1 sigma(g)+ <-- sigma(g)+ transition from the ground state is confirmed by the absence of J(odd) Q-branch lines in the resolved CARS spectrum. Analysis of this band in terms of a quasi-linear model gives a good fit to the observed transitions and leads to vibrational-rotational parameters (in cm(-1)) of nu1 = 2199.9773(12) and (B' - B'') = -2.044(6) x 10(-4). Other transitions originating from higher nu7 levels occur at only slightly lower wavenumber values and permit the calculation of the double minimum potential in the Q7 bending coordinate. The results indicate that the ground-state barrier to linearity (21.5 cm(-1)) increases by only 0.6 cm(-1) when the CO symmetric stretch is excited.

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