C. Smeenk

Partitioning of the Linear Photon Momentum in Multiphoton Ionization

The balance of the linear photon momentum in multiphoton ionization is studied experimentally. In the experiment argon and neon atoms are singly ionized by circularly polarized laser pulses with a wavelength of 800 and 1400 nm in the intensity range of 10(14)-10(15)  W/cm2. The photoelectrons are measured using velocity map imaging. We find that the photoelectrons carry linear momentum corresponding to the photons absorbed above the field free ionization threshold. Our finding has implications for concurrent models of the generation of terahertz radiation in filaments.

Momentum space tomographic imaging of photoelectrons

We apply tomography, a general method for reconstructing 3-D distributions from multiple projections, to reconstruct the momentum distribution of electrons produced via strong field photoionization. The projections are obtained by rotating the electron distribution via the polarization of the ionizing laser beam and recording a momentum spectrum at each angle with a 2-D velocity map imaging spectrometer. For linearly polarized light the tomographic reconstruction agrees with the distribution obtained using an Abel inversion. Electron tomography, which can be applied to any polarization, will simplify the technology of electron imaging. The method can be directly generalized to other charged particles.

Precise in-situ measurement of laser pulse intensity using strong field ionization

Building on the work of Alnaser et al. [Phys. Rev. A 70, 023413 (2004)], we devise an improved method for an in-situ measurement of the peak intensity in a focused, femtosecond infrared laser pulse. The method is shown to be effective with both photoion and photoelectron imaging devices. The model used to fit the experimental data has no unphysical free parameters used in fitting. The accuracy of the fit is 4% and the overall accuracy of the measurement is 8%.

Alignment Dependent Enhancement of the Photoelectron Cutoff for Multiphoton Ionization of Molecules

The multiphoton ionization rate of molecules depends on the alignment of the molecular axis with respect to the ionizing laser polarization. By studying molecular frame photoelectron angular distributions from N(2), O(2), and benzene, we illustrate how the angle-dependent ionization rate affects the photoelectron cutoff energy. We find alignment can enhance the high energy cutoff of the photoelectron spectrum when probing along a nodal plane or when ionization is otherwise suppressed. This is supported by calculations using a tunneling model with a single ion state.

Molecular alignment using circularly polarized laser pulses

We show that circularly polarized femtosecond laser pulses produce field-free alignment in linear and planar molecules. We study the rotational wavepacket evolution of O2 and benzene created by circularly polarized light. For benzene, we align the molecular plane to the plane of polarization. For O2, we demonstrate that circular polarization yields a net alignment along the laser propagation axis at certain phases of the evolution. Circular polarization gives us the ability to control alignment of linear molecules outside the plane of polarization, providing new capabilities for molecular imaging.

An STM for molecules and wide-bandgap crystal

We are all influenced by Nicolai Delone’s research. Through much of his career, his influence reached Canada through his published papers. However, Professor Delone visited the National Research Council of Canada’s laboratories at least three times from about 1989 to 1995. At that time he was primarily interested in stabilization. Stabilization refers to the fact that, as the intensity of laser light illuminating an atom is increased, the ionization rate passes through a maximum, then falls. Surprisingly the atom becomes stable against ionization at very high intensities.