Femtosecond Collisional Dissipation of Vibrating D_{2}

We explored the collision-induced vibrational decoherence of singly ionized D_{2} molecules inside a helium nanodroplet. By using the pump-probe reaction microscopy with few-cycle laser pulses, we captured in real time the collision-induced ultrafast dissipation of vibrational nuclear wave packet dynamics of D_{2}^{+} ion embedded in the droplet. Because of the strong coupling of excited molecular cations with the surrounding solvent, the vibrational coherence of D_{2}^{+} in the droplet interior only lasts for a few vibrational periods and completely collapses within 140 fs. The observed ultrafast coherence loss is distinct from that of isolated D_{2}^{+} in the gas phase, where the vibrational coherence persists for a long time with periodic quantum revivals. Our findings underscore the crucial role of ultrafast collisional dissipation in shaping the molecular decoherence and solvation dynamics during solution chemical reactions, particularly when the solute molecules are predominantly in ionic states.

Enhancing Strong-Field Dissociation of H_{2}

We investigate the above-threshold multiphoton ionization of H_{2} embedded in superfluid He nanodroplets driven by ultraviolet femtosecond laser pulses. We find that the surrounding He atoms enhance the dissociation of in-droplet H_{2}^{+} from lower vibrational states as compared to that of isolated gas-phase molecules. As a result, the discrete peaks in the photoelectron energy spectrum correlated with the HHe^{+} from the dissociative in-droplet molecule shift to higher energies. Based on the electron-nuclear correlation, the photoelectrons with higher energies are correlated to the nuclei of the low-vibrationally excited molecular ion as the nuclei share less photon energy. Our time-dependent nuclear wave packet quantum simulation using a simplified He-H_{2}^{+} system confirms the joint contribution of the driving laser field and the neighboring He atoms to the dissociation dynamics of the solute molecular ion. The results strengthen our understanding of the role of the environment on light-induced ultrafast dynamics of molecules.

Electron transfer in strong-field three-body fragmentation of ArKr2 trimers.

We experimentally studied the three-body fragmentation dynamics of a noble gas cluster (ArKr2) upon its multiple ionization by an intense femtosecond laser pulse. The three-dimensional momentum vectors of correlated fragmental ions were measured in coincidence for each fragmentation event. A novel comet-like structure was observed in the Newton diagram of the quadruple-ionization-induced breakup channel of ArKr2 4+→ Ar+ + Kr+ + Kr2+. The concentrated head part of the structure mainly originates from the direct Coulomb explosion process, while the broader tail part of the structure stems from a three-body fragmentation process involving electron transfer between the distant Kr+ and Kr2+ ion fragments. Due to the field-driven electron transfer, the Coulomb repulsive force of the Kr2+ and Kr+ ions with respect to the Ar+ ion undergoes exchange, leading to changes in the ion emission geometry in the Newton plot. An energy sharing among the separating Kr2+ and Kr+ entities was observed. Our study indicates a promising approach for investigating the strong-field-driven intersystem electron transfer dynamics by using the Coulomb explosion imaging of an isosceles triangle van der Waals cluster system.

Femtosecond Rotational Dynamics of D_{2} Molecules in Superfluid Helium Nanodroplets.

Rotational dynamics of D_{2} molecules inside helium nanodroplets is induced by a moderately intense femtosecond pump pulse and measured as a function of time by recording the yield of HeD^{+} ions, created through strong-field dissociative ionization with a delayed femtosecond probe pulse. The yield oscillates with a period of 185 fs, reflecting field-free rotational wave packet dynamics, and the oscillation persists for more than 500 periods. Within the experimental uncertainty, the rotational constant B_{He} of the in-droplet D_{2} molecule, determined by Fourier analysis, is the same as B_{gas} for an isolated D_{2} molecule. Our observations show that the D_{2} molecules inside helium nanodroplets essentially rotate as free D_{2} molecules.

Orbital effects in strong-field Rydberg state excitation of N2, Ar, O2 and Xe.

Rather than being freed to the continuum, the strong-field tunneled electrons can make a trajectory driven by the remaining laser fields and have certain probability to be captured by the high lying Rydberg states of the parent atoms or molecules. To explore the effect of molecular orbital on Rydberg state excitation, the ellipticity dependence of Rydberg state yields of N2 and O2 molecules are experimentally investigated using cold target recoil ion momentum spectroscopy and are compared with their counterpart atoms Ar and Xe with comparable ionization potentials. We found the generation probability of the neutral Rydberg fragment O2* was orders of magnitude higher than that of Xe* due to the butterfly-shaped highest occupied molecular orbital of O2. Meanwhile, our experimental and simulation results reveal that it is the initial momentum distribution (determined by the detailed characteristics of orbitals) that finally leads to the tendency that the Rydberg state yield of O2 (Ar) decreased slower than that obtained for Xe (N2) when the ellipticity of the excitation laser field is increased.

Clocking Dissociative Above-Threshold Double Ionization of H_{2} in a Multicycle Laser Pulse.

The dissociative above-threshold double ionization (ATDI) of H_{2} in strong laser fields involves the sequential releasing of two electrons at specific instants with the stretching of the molecular bond. By mapping the releasing instants of two electrons to their emission directions in a multicycle polarization-skewed femtosecond laser pulse, we experimentally clock the dissociative ATDI of H_{2} via distinct photon-number-resolved pathways, which are distinguished in the kinetic energy release spectrum of two protons measured in coincidence. The timings of the experimentally resolved dissociative ATDI pathways are in good accordance with the classical predictions. Our results verify the multiphoton scenario of the dissociative ATDI of H_{2} in both time and energy fashion, strengthening the understanding of the strong-field phenomenon and providing a robust tool with a subcycle time resolution to clock abundant ultrafast dynamics of molecules.

Visualizing and Steering Dissociative Frustrated Double Ionization of Hydrogen Molecules.

We experimentally visualize the dissociative frustrated double ionization of hydrogen molecules by using few-cycle laser pulses in a pump-probe scheme, in which process the tunneling ionized electron is recaptured by one of the outgoing nuclei of the breaking molecule. Three internuclear distances are recognized to enhance the dissociative frustrated double ionization of molecules at different instants after the first ionization step. The recapture of the electron can be further steered to one of the outgoing nuclei as desired by using phase-controlled two-color laser pulses. Both the experimental measurements and numerical simulations suggest that the Rydberg atom is favored to emit to the direction of the maximum of the asymmetric optical field. Our results on the one hand intuitively visualize the dissociative frustrated double ionization of molecules, and on the other hand open the possibility to selectively excite the heavy fragment ejected from a molecule.

Ultrafast photoinduced C-H bond formation from two small inorganic molecules.

The formation of carbon-hydrogen (C-H) bonds via the reaction of small inorganic molecules is of great significance for understanding the fundamental transition from inorganic to organic matter, and thus the origin of life. Yet, the detailed mechanism of the C-H bond formation, particularly the time scale and molecular-level control of the dynamics, remain elusive. Here, we investigate the light-induced bimolecular reaction starting from a van der Waals molecular dimer composed of two small inorganic molecules, H2 and CO. Employing reaction microscopy driven by a tailored two-color light field, we identify the pathways leading to C-H photobonding thereby producing HCO+ ions, and achieve coherent control over the reaction dynamics. Using a femtosecond pump-probe scheme, we capture the ultrafast formation time, i.e., 198 ± 16 femtoseconds. The real-time visualization and coherent control of the dynamics contribute to a deeper understanding of the most fundamental bimolecular reactions responsible for C-H bond formation, thus contributing to elucidate the emergence of organic components in the universe.

Ultrafast formation dynamics of D3+ from the light-driven bimolecular reaction of the D2-D2 dimer.

The light-driven formation of trihydrogen cation has been attracting considerable attention because of its important role as an initiator of chemical reactions in interstellar clouds. To understand the formation dynamics, most previous studies focused on creating H3+ or D3+ from unimolecular reactions of various organic molecules. Here we observe and characterize the ultrafast formation dynamics of D3+ from a bimolecular reaction, using pump-probe experiments that employ ultrashort laser pulses to probe its formation from a D2-D2 dimer. Our molecular dynamics simulations provide an intuitive representation of the reaction dynamics, which agree well with the experimental observation. We also show that the emission direction of D3+ can be controlled using a tailored two-colour femtosecond laser field. The underlying control mechanism is in line with what is known from the light control of electron localization in the bond breaking of single molecules.

Stereodynamical Control of D3+ Formation from the Bimolecular Photoreaction in the D2-D2 Dimer.

We report the stereodynamic control of D3+ formation from the laser-induced bimolecular reaction in a weakly bound D2-D2 dimer via impulsive molecular alignment. Using a linearly polarized moderately intense femtosecond pump pulse, the D2 molecules in the dimer were prealigned prior to the bimolecular reaction triggered by a delayed probe pulse. The rotationally excited D2 in the dimer was observed to rotate freely as if it were a monomer. It was demonstrated that the yield of photoreaction product D3+ is increased or decreased when the molecular axis of D2 is parallel or perpendicular to the probe laser polarization, respectively. The underlying physics of this steric effect is the alignment-dependent bond cleavage of D2+ in the dimer induced by a photon-coupled parallel transition.

Atomic partial wave meter by attosecond coincidence metrology.

Attosecond chronoscopy is central to the understanding of ultrafast electron dynamics in matter from gas to the condensed phase with attosecond temporal resolution. It has, however, not yet been possible to determine the timing of individual partial waves, and steering their contribution has been a substantial challenge. Here, we develop a polarization-skewed attosecond chronoscopy serving as a partial wave meter to reveal the role of each partial wave from the angle-resolved photoionization phase shifts in rare gas atoms. We steer the relative ratio between different partial waves and realize a magnetic-sublevel-resolved atomic phase shift measurement. Our experimental observations are well supported by time-dependent R-matrix numerical simulations and analytical soft-photon approximation analysis. The symmetry-resolved, partial-wave analysis identifies the transition rate and phase shift property in the attosecond photoelectron emission dynamics. Our findings provide critical insights into the ubiquitous attosecond optical timer and the underlying attosecond photoionization dynamics.

Femtosecond Resolving Photodissociation Dynamics of the SO2 Molecule.

We experimentally investigate the ultrafast photodissociation dynamics of the SO2 molecule induced by intense ultrashort laser pulses in a pump-probe scheme. Different three-body fragmentation pathways are discriminated using the time-dependent kinetic energy release spectrum with femtosecond time resolution. A nontrivial three-body fragmentation pathway, denoted as the bonding pathway, is unraveled, in which an intermediate fast rotating O2 molecule is formed before complete fragmentation. The ultrafast chemical bond rearrangement after electron release is tracked in real time. The bonding pathway generally exists in the three-body fragmentation processes induced by strong laser fields of different wavelengths, which is observed in infrared, ultraviolet, and mixed two-color cases. Our findings are significant for understanding the photon-induced ultrafast processes of the SO2 molecule in atmospheric chemistry.

Electron-nuclear correlated multiphoton-route to Rydberg fragments of molecules.

Atoms and molecules exposed to strong laser fields can be excited to the Rydberg states with very high principal quantum numbers and large orbitals. It allows acceleration of neutral particles, generate near-threshold harmonics, and reveal multiphoton Rabi oscillations and rich photoelectron spectra. However, the physical mechanism of Rydberg state excitation in strong laser fields is yet a puzzle. Here, we identify the electron-nuclear correlated multiphoton excitation as the general mechanism by coincidently measuring all charged and neutral fragments ejected from a H2 molecule. Ruled by the ac-Stark effect, the internuclear separation for resonant multiphoton excitation varies with the laser intensity. It alters the photon energy partition between the ejected electrons and nuclei and thus leads to distinct kinetic energy spectra of the nuclear fragments. The electron-nuclear correlation offers an alternative visual angle to capture rich ultrafast processes of complex molecules.

All-optical field-free three-dimensional orientation of asymmetric-top molecules.

Orientation and alignment of molecules by ultrashort laser pulses is crucial for a variety of applications and has long been of interest in physics and chemistry, with the special emphasis on stereodynamics in chemical reactions and molecular orbitals imaging. As compared to the laser-induced molecular alignment, which has been extensively studied and demonstrated, achieving molecular orientation is a much more challenging task, especially in the case of asymmetric-top molecules. Here, we report the experimental demonstration of all-optical field-free three-dimensional orientation of asymmetric-top molecules by means of phase-locked cross-polarized two-color laser pulse. This approach is based on nonlinear optical mixing process caused by the off-diagonal elements of the molecular hyperpolarizability tensor. It is demonstrated on SO2 molecules and is applicable to a variety of complex nonlinear molecules.