Photoionization is a complex quantum mechanical process, with a range of interfering channels playing a role in even the simplest case. For problems in quantum metrology and sensing, a detailed understanding of the process is desirable for accurate measurements; quantum control is also a possible outcome of such understanding. New research in this area will build on recent cutting-edge work at NRC (see below), which probed the fundamental quantum physics of photoionization in atoms and molecules, and metrology work which demonstrated the retrieval of electron wavefunctions via interferometric time-domain measurements.
Four areas of photoionization interferometry are the target of current research:
- Metrology and control with rotational wavepackets.
- Metrology and control with shaped laser pulses.
- Quantum dynamics probed via photoionization interferometry.
- Fundamental properties of photoion and photoelectron coherence.
Depending on interests and experience, project work will be in one (or more) of these areas.
An introduction to this topic, and recent work, can be found in Paul’s DAMOP 2017 talk Phase-sensitive Photoelectron Metrology (below), and via our blog.
Slides for Paul’s DAMOP talk are now available on figshare (DOI: 10.6084/m9.figshare.5049142).
Photoionization is an interferometric process, in which multiple paths can contribute to the final continuum photoelectron state. At the simplest level, interferences between different final angular momentum states are manifest in the energy and angle resolved photoelectron spectra: metrology schemes making use of these interferograms are thus phase-sensitive, and provide a powerful route to detailed understanding of photoionization . At a more complex level, such measurements can also provide a powerful probe for other processes of interest, for example: (a) dynamical process in time-resolved measurements, such as rotational, vibrational and electronic wavepackets, and (b) in order to understand and develop control schemes . In this talk recent work in this vein will be discussed, touching on “complete” photoionization studies of atoms and molecules with shaped laser pulses [1,2] and XUV , metrology schemes using Angle-Resolved RABBIT, and molecular photoionization dynamics in the time-domain (Wigner delays) .
 Hockett, P. et. al. (2015). Phys. Rev. A, 92, 13412.  Hockett, P. et. al. (2014). Phys. Rev. Lett., 112, 223001.  Marceau, C. et. al. (2017). Submitted. DOI: 10.6084/m9.figshare.4480349.  Hockett, P. et. al. (2016). J. Phys B, 49, 95602.
Update 29th June 2017 – a video of the talk is now also available.
Our ongoing work on the calculation of time-dependent wavepackets and observables in photoionization is now collected in an OSF project (DOI: 10.17605/OSF.IO/RJMPD). Aspects of this work have previously been published, but much of the detail and methodology underlying the calculations has remained sitting on our computers. As part of our Open Science Initiative, we’re letting this data go free! Head over to the OSF project “Time-dependent Wavepackets and Photoionization – CS2” for more.
Figure shows TRPADs results (a) Calculated TRPADs (0.7eV) (b), (c) Comparison with expt. TRPADs (discrete times).
Our latest work with the PImMS camera, femtosecond VUV pulses, and velocity-map imaging, has been picked up for a press release by AIP.
The Inner Lives of Molecules
New method takes 3-D images of molecules in action
WASHINGTON, D.C., April 4, 2017 — Quantum mechanics rules. It dictates how particles and forces interact, and thus how atoms and molecules work — for example, what happens when a molecule goes from a higher-energy state to a lower-energy one. But beyond the simplest molecules, the details become very complex.
“Quantum mechanics describes how all this stuff works,” said Paul Hockett of the National Research Council of Canada. “But as soon as you go beyond the two-body problem, you can’t solve the equations.” So, physicists must rely on computer simulations and experiments.
Now, he and an international team of researchers from Canada, the U.K. and Germany have developed a new experimental technique to take 3-D images of molecules in action. This tool, he said, can help scientists better understand the quantum mechanics underlying bigger and more complex molecules.
The new method, described in The Journal of Chemical Physics, from AIP Publishing, combines two technologies. The first is a camera developed at Oxford University, called the Pixel-Imaging Mass Spectrometry (PImMS) camera. The second is a femtosecond vacuum ultraviolet light source built at the NRC femtolabs in Ottawa.
Mass spectrometry is a method used to identify unknown compounds and to probe the structure of molecules. In most types of mass spectrometry, a molecule is fragmented into atoms and smaller molecules that are then separated by molecular weight. In time-of-flight mass spectrometry, for example, an electric field accelerates the fragmented molecule. The speed of those fragments depends on their mass and charge, so to weigh them, you measure how long it takes for them to hit the detector.
Most conventional imaging detectors, however, can’t discern exactly when one particular particle hits. To measure timing, researchers must use methods that effectively act as shutters, which let particles through over a short time period. Knowing when the shutter is open gives the time-of-flight information. But this method can only measure particles of the same mass, corresponding to the short time the shutter is open.
The PImMS camera, on the other hand, can measure particles of multiple masses all at once. Each pixel of the camera’s detector can time when a particle strikes it. That timing information produces a three-dimensional map of the particles’ velocities, providing a detailed 3-D image of the fragmentation pattern of the molecule.
To probe molecules, the researchers used this camera with a femtosecond vacuum ultraviolet laser. A laser pulse excites the molecule into a higher-energy state, and just as the molecule starts its quantum mechanical evolution — after a few dozen femtoseconds –another pulse is fired. The molecule absorbs a single photon, a process that causes it to fall apart. The PImMS camera then snaps a 3-D picture of the molecular debris.
By firing a laser pulse at later and later times at excited molecules, the researchers can use the PImMS camera to take snapshots of molecules at various stages while they fall into lower energy states. The result is a series of 3-D blow-by-blow images of a molecule changing states.
The researchers tested their approach on a molecule called C2F3I. Although a relatively small molecule, it fragmented into five different products in their experiments. The data and analysis software is available online as part of an open science initiative, and although the results are preliminary, Hockett said, the experiments demonstrate the power of this technique.
“It’s effectively an enabling technology to actually do these types of experiments at all,” Hockett said. It only takes a few hours to collect the kind of data that would take a few days using conventional methods, allowing for experiments with larger molecules that were previously impossible.
Then researchers can better answer questions like: How does quantum mechanics work in larger, more complex systems? How do excited molecules behave and how do they evolve?
“People have been trying to understand these things since the 1920s,” Hockett said. “It’s still a very open field of investigation, research, and debate because molecules are really complicated. We have to keep trying to understand them.”
The article, Time-resolved multi-mass ion imaging: femtosecond UV-VUV pump-probe spectroscopy with the PImMS camera, is now published in the Journal of Chemical Physics, and also available via the arXiv 1702.00744 and Authorea (original text), DOI: 10.22541/au.149030711.19068540.
The full dataset and analysis scripts are available via OSF, DOI: 10.17605/OSF.IO/RRFK3.
New on the arxiv:
ePSproc: Post-processing suite for ePolyScat electron-molecule scattering calculations
ePSproc provides codes for post-processing results from ePolyScat (ePS), a suite of codes for the calculation of quantum scattering problems, developed and released by Luchesse & co-workers (Gianturco et al. 1994)(Natalense and Lucchese 1999)(R. R. Lucchese and Gianturco 2016). ePS is a powerful computational engine for solving scattering problems, but its inherent complexity, combined with additional post-processing requirements, ranging from simple visualizations to more complex processing involving further calculations based on ePS outputs, present a significant barrier to use for most researchers. ePSproc aims to lower this barrier by providing a range of functions for reading, processing and plotting outputs from ePS. Since ePS calculations are currently finding multiple applications in AMO physics (see below), ePSproc is expected to have significant reuse potential in the community, both as a basic tool-set for researchers beginning to use ePS, and as a more advanced post-processing suite for those already using ePS. ePSproc is currently written for Matlab/Octave, and distributed via Github: https://github.com/phockett/ePSproc.
Malte C Tichy, Florian Mintert and Andreas Buchleitner
Published 21 September 2011 • 2011 IOP Publishing Ltd
Entanglement is nowadays considered as a key quantity for the understanding of correlations, transport properties and phase transitions in composite quantum systems, and thus receives interest beyond the engineered applications in the focus of quantum information science. We review recent experimental and theoretical progress in the study of quantum correlations under that wider perspective, with an emphasis on rigorous definitions of the entanglement of identical particles, and on entanglement studies in atoms and molecules.
New article in the Journal of Modern Optics
A snippet from some theory work in progress on time delays in molecular photoionization. The image below shows the energy and angle-resolved cross-section (surface topography) and Wigner delay (colour map) over a 40 eV range for CO. Unsurprisingly, for a molecular scatterer (albeit a simple heteronuclear diatomic) the map is quite complicated! Here the delays range from -200 to +200 attoseconds, and peak at the Carbon end of the molecule.
More on this soon… the paper is almost ready…
UPDATE Dec. 2015
Now on the arXiv:
P. Hockett, E. Frumker, D.M. Villeneuve, P.B. Corkum
arXiv 1512.03788, 2015