Nora G. Kling

Subfemtosecond steering of hydrocarbon deprotonation through superposition of vibrational modes

Subfemtosecond control of the breaking and making of chemical bonds in polyatomic molecules is poised to open new pathways for the laser-driven synthesis of chemical products. The break-up of the C-H bond in hydrocarbons is an ubiquitous process during laser-induced dissociation. While the yield of the deprotonation of hydrocarbons has been successfully manipulated in recent studies, full control of the reaction would also require a directional control (that is, which C-H bond is broken). Here, we demonstrate steering of deprotonation from symmetric acetylene molecules on subfemtosecond timescales before the break-up of the molecular dication. On the basis of quantum mechanical calculations, the experimental results are interpreted in terms of a novel subfemtosecond control mechanism involving non-resonant excitation and superposition of vibrational degrees of freedom. This mechanism permits control over the directionality of chemical reactions via vibrational excitation on timescales defined by the subcycle evolution of the laser waveform.

Carrier-Envelope Phase Control over Pathway Interference in Strong-Field Dissociation of H2+

The dissociation of an H2+ molecular-ion beam by linearly polarized, carrier-envelope-phase-tagged 5 fs pulses at 4×10(14) W/cm2 with a central wavelength of 730 nm was studied using a coincidence 3D momentum imaging technique. Carrier-envelope-phase-dependent asymmetries in the emission direction of H+ fragments relative to the laser polarization were observed. These asymmetries are caused by interference of odd and even photon number pathways, where net zero-photon and one-photon interference predominantly contributes at H+ + H kinetic energy releases of 0.2-0.45 eV, and net two-photon and one-photon interference contributes at 1.65-1.9 eV. These measurements of the benchmark H2+ molecule offer the distinct advantage that they can be quantitatively compared with ab initio theory to confirm our understanding of strong-field coherent control via the carrier-envelope phase.

Steering Proton Migration in Hydrocarbons Using Intense Few-Cycle Laser Fields

Proton migration is a ubiquitous process in chemical reactions related to biology, combustion, and catalysis. Thus, the ability to manipulate the movement of nuclei with tailored light within a hydrocarbon molecule holds promise for far-reaching applications. Here, we demonstrate the steering of hydrogen migration in simple hydrocarbons, namely, acetylene and allene, using waveform-controlled, few-cycle laser pulses. The rearrangement dynamics is monitored using coincident 3D momentum imaging spectroscopy and described with a widely applicable quantum-dynamical model. Our observations reveal that the underlying control mechanism is due to the manipulation of the phases in a vibrational wave packet by the intense off-resonant laser field.

Carrier-envelope phase dependence of the directional fragmentation and hydrogen migration in toluene in few-cycle laser fields.

The dissociative ionization of toluene initiated by a few-cycle laser pulse as a function of the carrier envelope phase (CEP) is investigated using single-shot velocity map imaging. Several ionic fragments, CH3+, H2+, and H3+, originating from multiply charged toluene ions present a CEP-dependent directional emission. The formation of H2+ and H3+ involves breaking C-H bonds and forming new bonds between the hydrogen atoms within the transient structure of the multiply charged precursor. We observe appreciable intensity-dependent CEP-offsets. The experimental data are interpreted with a mechanism that involves laser-induced coupling of vibrational states, which has been found to play a role in the CEP-control of molecular processes in hydrocarbon molecules, and appears to be of general importance for such complex molecules.

Single-Cycle Non-Sequential Double Ionization

Non-sequential double ionization (NSDI) is a process in which two electrons are ripped off an atom or molecule by a strong laser field in a correlated manner. Although NSDI has been the subject of numerous experimental and theoretical studies over the past three decades, the exact mechanisms responsible for the observed energy and momentum sharing between the electrons generated in the process, are not yet fully understood. The main reason lies in the fact that the theoretical description of the complex correlated many body dynamics that govern NSDI is exceedingly difficult. A particularly challenging task for theory is the modeling of NSDI dynamics over time scales exceeding one period of the laser field. As a result, most calculations are restricted to a single laser cycle. On the experimental side, in contrast, kinematically complete experiments on single-cycle NSDI has long been prohibitively challenging. Therefore, the comparison between theory and experiments has been limited, so far, to a very qualitative level. We review recent results obtained from first kinematically complete NSDI experiments in the single cycle regime. We illustrate the insight gained from these experiments, and discuss how the new experimental data may facilitate verification of theoretical models on a quantitative level.

Thick-lens velocity-map imaging spectrometer with high resolution for high-energy charged particles

A novel design for a velocity-map imaging (VMI) spectrometer with high resolution over a wide energy range surpassing a standard VMI design is reported. The main difference to a standard three-electrode VMI is the spatial extension of the applied field using 11 electrodes forming a thick-lens. This permits measurements of charged particles with higher energies while achieving excellent resolving power over a wide range of energies. Using SIMION simulations, the thick-lens VMI is compared to a standard design for up to 360 eV electrons. The simulations also show that the new spectrometer design is suited for charged-particle detection with up to 1 keV using a repeller-electrode voltage of -30 kV. The experimental performance is tested by laser-induced ionization of rare gases producing electrons up to about 70 eV. The thick-lens VMI is useful for a wide variety of studies on atoms, molecules and nanoparticles in intense laser fields and high-photon-energy fields from high-harmonic-generation or free-electron lasers.

Elucidating isotopic effects in intense ultrafast laser-driven D2H+ fragmentation

The triatomic hydrogen molecular ion is instrumental as a benchmark towards understanding the strong-field dynamics of polyatomic molecules. Using a crossed-beams coincidence three-dimensional momentum imaging method, we demonstrate clear isotopic effects in the fragmentation of D2H+ induced by 7 fs (40 fs), 790?nm laser pulses at an intensity of 1016 W cm?2 (5 ? 1015 W cm?2). Our experiment uniquely separates all fragmentation channels and provides kinematically complete information for the nuclear fragments. For example, we show that for dissociative ionization of D2H+ there is a large difference in branching ratios of the two-body channels, namely, H++D dominates D++HD+, whereas there is minimal difference in branching ratios between the dissociation channels H++D2 and D++HD.

Visualization of bond rearrangements in acetylene using near single-cycle laser pulses

The migration of hydrogen atoms resulting in the isomerization of hydrocarbons is an important process which can occur on ultrafast timescales. Here, we visualize the light-induced hydrogen migration of acetylene to vinylidene in an ionic state using two synchronized 4 fs intense laser pulses. The first pulse induces hydrogen migration, and the second is used for monitoring transient structural changes via Coulomb explosion imaging. Varying the time delay between the pulses reveals the migration dynamics with a time constant of 54 ± 4 fs as observed in the H+ + H+ + CC+ channel. Due to the high temporal resolution, vibrational wave-packet motions along the CC- and CH-bonds are observed. Even though a maximum in isomerization yield for kinetic energy releases above 16 eV is measured, we find no indication for a backwards isomerization - in contrast to previous measurements. Here, we propose an alternative explanation for the maximum in isomerization yield, namely the surpassing of the transition state to the vinylidene configuration within the excited dication state.

Non-sequential double ionization of Ar: from the single-to the many-cycle regime

The transition from the near-single to the multi-cycle regime in non-sequential double ionization of argon is investigated experimentally. Argon atoms are exposed to intense laser pulses with a center wavelength around 790 nm and the momenta of electrons and ions generated in the double ionization process are measured in coincidence using a reaction microscope. The duration of the near transform-limited pulses is varied from 4 to 30 fs. We observe an abrupt collapse of the cross-shaped two-electron momentum distribution [17] in the few-cycle regime. The transition to longer pulses is further accompanied by a strong increase in the fraction of anti-correlated to correlated electrons.

Sub-cycle steering of the deprotonation of acetylene by intense few-cycle mid-infrared laser fields

Directional breaking of the C-H/C-D molecular bond is manipulated in acetylene (C2H2) and deuterated acetylene (C2D2) by waveform controlled few-cycle mid-infrared laser pulses with a central wavelength around 1.6 μm at an intensity of about 8 × 1013 W/cm2. The directionality of the deprotonation of acetylene is controlled by changing the carrier-envelope phase (CEP). The CEP-control can be attributed to the laser-induced superposition of vibrational modes, which is sensitive to the sub-cycle evolution of the laser waveform. Our experiments and simulations indicate that near-resonant, intense mid-infrared pulses permit a higher degree of control of the directionality of the reaction compared to those obtained in near-infrared fields, in particular for the deuterated species.