We report the first experimental observation of nonadiabatic field-free orientation of a heteronuclear diatomic molecule (CO) induced by an intense two-color (800 and 400 nm) femtosecond laser field. We monitor orientation by measuring fragment ion angular distributions after Coulomb explosion with an 800 nm pulse. The orientation of the molecules is controlled by the relative phase of the two-color field. The results are compared to quantum mechanical rigid rotor calculations. The demonstrated method can be applied to study molecular frame dynamics under field-free conditions in conjunction with a variety of spectroscopy methods, such as high-harmonic generation, electron diffraction, and molecular frame photoelectron emission.

Abstract:We study the evolution of nuclear wave packets launched in molecular nitrogen, oxygen and carbon monoxide by intense 8fs infrared pulses.We use velocity map imaging to measure the momentum of the ion fragments when these wave packets are interrogated by a second such pulse after a variable time delay. Both quasi-bound and dissociative wave packets are observed. For the former, measurements of bound-state oscillations are used to identify the participating states and in some cases extract properties of the relevant potential energy surfaces. Vibrational structure is resolved in both energy and oscillation-frequency for the cations of oxygen and carbon monoxide, displaying the same quantum wave packet motion in both energy and time domains. In addition, vibrational structure is seen in the dication of carbon 2 monoxide in a situation where the energy resolution by itself is inadequate to resolve the structure.

In 1997, it was predicted that an electronically excited atom or molecule placed in a loosely bound chemical system (such as a hydrogen-bonded or van-der-Waals-bonded cluster) could efficiently decay by transferring its excess energy to a neighbouring species that would then emit a low-energy electron. This intermolecular Coulombic decay (ICD) process has since been shown to be a common phenomenon, raising questions about its role in DNA damage induced by ionizing radiation, in which low-energy electrons are known to play an important part. It was recently suggested that ICD can be triggered efficiently and site-selectively by resonantly core-exciting a target atom, which then transforms through Auger decay into an ionic species with sufficiently high excitation energy to permit ICD to occur. Here we show experimentally that resonant Auger decay can indeed trigger ICD in dimers of both molecular nitrogen and carbon monoxide. By using ion and electron momentum spectroscopy to measure simultaneously the charged species created in the resonant-Auger-driven ICD cascade, we find that ICD occurs in less time than the 20 femtoseconds it would take for individual molecules to undergo dissociation. Our experimental confirmation of this process and its efficiency may trigger renewed efforts to develop resonant X-ray excitation schemes for more localized and targeted cancer radiation therapy.

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The process by which a molecule in an intense laser field ionizes more efficiently as its bond length increases towards a critical distance R(c) is known as charge resonance enhanced ionization (CREI). We make a series of measurements of this process for CO(2), by varying pulse duration from 7 to 200 fs, in order to identify the charge states and time scales involved. We find that for the 4+ and higher charge states, 100 fs is the time scale required to reach the critical geometry ≈ 2.1 Å and <θ(OCO)> ≈ 163° (equilibrium CO(2) geometry is ≈ 1.16 Å and <θ(OCO)> ≈ 172°). The CO(2)(3+) molecule, however, appears always to begin dissociation from closer than 1.7 Å indicating that dynamics on charge states lower than 3+ is not sufficient to initiate CREI. Finally, we make quantum ab initio calculations of ionization rates for CO(2) and identify the electronic states responsible for CREI.

We have measured full momentum images of electrons rescattered from Xe, Kr, and Ar following the liberation of the electrons from these atoms by short, intense laser pulses. At high momenta the spectra show angular structure (diffraction) which is very target dependent and in good agreement with calculated differential cross sections for the scattering of free electrons from the corresponding ionic cores.

We demonstrate a method for determining the full three-dimensional molecular-frame photoelectron angular distribution in polyatomic molecules using methane as a prototype. Simultaneous double Auger decay and subsequent dissociation allow measurement of the initial momentum vectors of the ionic fragments and the photoelectron in coincidence, allowing full orientation by observing a three-ion decay pathway, (H þ , H þ , CH þ 2 ). We find the striking result that at low photoelectron energies the molecule is effectively imaged by the focusing of photoelectrons along bond directions. DOI: 10.1103/PhysRevLett.108.233002 PACS numbers: 33.80.Eh, 33.60.+q Imaging molecular structure is a critical challenge in chemical physics recently highlighted by the emergence of techniques that, similar to ultrafast electron diffraction [1] or x-ray diffraction [2], have the potential to be taken to the time domain and thereby ultimately be used to make ''movies'' of chemical reactions on their natural time scale. Of particular interest is the development of such techniques that can be applied to the dynamics of isolated molecules. Here, the full three-dimensional orientation of a polyatomic molecule is measured simultaneously with the three components of the momentum of a photoelectron ejected from it with no underlying assumptions of symmetry or geometry. We present three-dimensional images of a polyatomic molecule measured with this technique, demonstrating an effect predicted [3] for polyatomic molecules with a heavy central atom bonded to hydrogens, namely that low-energy photoelectrons can directly image the molecular potential and bond structure.When a photoelectron is launched by photoabsorption of an inner shell, the outgoing photoelectron wave is then scattered by the aggregate potential of the molecule. The final angular distribution in the body-fixed frame of the molecule is an exquisitely sensitive probe of molecular structure and initial electronic state, which has been recently argued and demonstrated [4,5]. However, observing molecular-frame photoelectron angular distributions (MFPADs) at high resolution requires accurate orientation of the molecule in the gas phase. Three-dimensional laser alignment [6,7] can accomplish such orientation prior to photoionization but is limited to molecules with an asymmetric polarizability. In the case of simple diatomic molecules, orientation can also be accomplished by detecting the photoelectron in coincidence with positively charged fragments that emerge following prompt Auger decay and dissociation [8]. Progress has also been made toward threedimensional MFPAD measurement using coincidence detection and velocity map imaging [9]. Here we present photoelectron imaging of methane molecules, where both the photoelectron momentum and corresponding body frame of the polyatomic molecule are fully determined in all three dimensions.For many molecules, including CH 4 , core ionization opens a strong simultaneous double Auger decay channel that produces a trication that then can disso...

Secondary electrons play critical roles in several imaging technologies, including extreme ultraviolet (EUV) lithography. At longer wavelengths of light (e.g. 193 and 248 nm), the photons are directly involved in the photochemistry occurring during photolysis. EUV light (13.5 nm, 92 eV), however, first creates a photoelectron, and this electron, or its subsequent daughter electrons create most of the chemical changes that occur during exposure. Despite the importance of these electrons, the details surrounding the chemical events leading to acid production remain poorly understood. Previously reported experimental results using high PAG-loaded resists have demonstrated that up to five or six photoacids can be generated per incident photon. Until recently, only electron recombination events were thought to play a role in acid generation, requiring that at least as many secondary electrons are produced to yield a given number of acid molecules. However, the initial results we have obtained using a Monte Carlo-based modeling program, LESiS, demonstrate that only two to three secondary electrons are made per absorbed EUV photon. A more comprehensive understanding of EUVinduced acid generation is therefore needed for the development of higher performance resists.