The size-dependent strong-field ionization and dissociation dynamics of (H$_2$O)$_n$ (n=1-4) are investigated using real-time time-dependent density functional theory (RT-TDDFT) coupled to Ehrenfest molecular dynamics under a common few-cycle near-infrared laser pulse. It is found that the net ionization per monomer varies only weakly on cluster size, whereas the protonic and oxygen response is changed much more strongly once the cluster size grows beyond the dimer. In particular, H-ejection activity is observed to rise sharply from the dimer to the trimer/tetramer regime, while stable H-transfer is essentially absent in the dimer under the present criterion but becomes substantial in the trimer and is further amplified in the tetramer. Through timing analyses, it is shown that the dimer exhibits a weak and temporally broad response, whereas the larger clusters display a much stronger early-time protonic response concentrated within and immediately after the laser pulse window. By endpoint oxygen statistics, a systematic increase in dissociation propensity with cluster size is likewise shown. For a clean subset of direct two-body dimer breakup trajectories, the asymptotic kinetic energy release is estimated to be 4.47 $\pm$ 1.03 eV, in reasonably good agreement with the experimental value for the unprotonated two-body Coulomb-explosion channel. Overall, it is shown by the results that increasing water-cluster size primarily reshapes the strong-field response through proton-mediated and topology-level nuclear dynamics rather than through a large change in net ionization alone.
The dissociation energy of H$_2$ represents a benchmark quantity to test the accuracy of first-principles calculations. We present a new measurement of the energy interval between the EF $^1Σ_g^+(v=0,N=1)$ state and the 54p1$_1$ Rydberg state of H$_2$. When combined with previously determined intervals, this new measurement leads to an improved value of the dissociation energy $D_0^{N=1}$ of ortho-H$_2$ that has, for the first time, reached a level of uncertainty that is three times smaller than the contribution of about 1 MHz resulting from the finite size of the proton. The new result of 359…
Based on a combined quantum-classical treatment, a complete study of the strong field dynamics of H2+, i.e. including all nuclear and electronic DOF as well as dissociation and ionization, is presented. We find that the ro-vibrational nuclear dynamics enhances dissociation and, at the same time, suppresses ionization, confirming experimental observations by I. Ben-Itzhak et al. [Phys. Rev. Lett. 95, 073002 (2005)]. In addition and counter-intuitively, it is shown that for large initial vibrational excitation ionization takes place favorably at large angles between the laser polarization and mo…
We investigate the dissociation and ionization equilibria of deuterium fluid over a wide range of temperatures and densities. The partition functions for molecular and atomic species are evaluated, in a statistical-mechanically consistent way, implementing recent developments in the literature and taking high-density effects into account. A new chemical model (free energy function) is introduced in which the fluid is considered as a mixture of diatomic molecules, atoms, ions and free electrons. Intensive short range hard core repulsion is taken into account together with partial degeneracy of …
Polyatomic molecules in strong laser fields can undergo substantial nuclear motion within tens of femtoseconds. Ion imaging methods based on dissociation or Coulomb explosion therefore have difficulty faithfully recording the geometry dependence of the field ionization that initiates the dissociation process. Here we compare the strong-field double ionization and subsequent dissociation of water (both H$_2$O and D$_2$O) in 10-fs and 40-fs 800-nm laser pulses. We find that 10-fs pulses turn off before substantial internuclear motion occurs, whereas rapid internuclear motion can take place durin…
Löwdin's symmetry dilemma is an ubiquitous issue in approximate quantum chemistry. In the context of Hartree-Fock (HF) theory, the use of Slater determinants with some imposed constraints to preserve symmetries of the exact problem may lead to physically unreasonable potential energy surfaces. On the other hand, lifting these constraints leads to the so-called broken symmetry solutions that usually provide better energetics, at the cost of losing information about good quantum numbers that describe the state of the system. This behavior has been previously extensively studied in the context of…
We have studied strong-field enhanced dissociative ionization of D$_{2}$O in 40 fs, 800 nm laser pulses with focused intensities of $< 1 - 3 \times 10^{15}W/cm^2$ by resolving the charged fragment momenta with respect to the laser polarization. We observe dication dissociation into OD$^{+}$/D$^{+}$ dominates when the polarization is out of the plane of the molecule, whereas trication dissociation into O$^{+}$/D$^{+}$/D$^{+}$ is strongly dominant when the polarization is aligned along the D-D axis. Dication dissociation into O/D$^{+}$/D$^{+}$, and O$^{+}$/D$_2$$^{+}$ is not seen, nor is there a…
We present state-selective measurements on the NH$_2^{+}$ + H$^{+}$ and NH$^{+}$ + H$^{+}$ + H dissociation channels following single-photon double ionization at 61.5 eV of neutral NH$_{3}$, where the two photoelectrons and two cations are measured in coincidence using 3-D momentum imaging. Three dication electronic states are identified to contribute to the NH$_2^{+}$ + H$^{+}$ dissociation channel, where the excitation in one of the three states undergoes intersystem crossing prior to dissociation, producing a cold NH$_2^+$ fragment. In contrast, the other two states directly dissociate, pro…
We show the details of the pathway for dissociative ionization process of ground electronic state of aligned D$^{+}_{2}$ due to first ionization of D$_2$ in short ($\thicksim$100 fs) and intense ($4.0\times10^{14}$ W cm$^{-2}$) 480 nm laser pulses. The initial vibrational state of D$^{+}_{2}$ comes from the vertical transformation of the ground state of D$_{2}$. The initial wavepacket in the ground electronic state of D$_{2}^{+}$ is outgoing through dissociation-ionization channel accompanied by a strong coupling between $1s σ_{g}$ and $2p σ_{u}$ electronic states. We show explicitly that the …
In strong field ionization, the pump pulse not only photoionizes the molecule, but also drives efficient population exchanges between its ionic ground and excited states.In this study, we investigated the population dynamics accompanying strong field molecular photoionization, using angular distribution of dissociative fragments after ionization.Our results reveal that the first and higher order processes of the post-ionization population redistribution mechanism (PPRM) in the ion core can be disentangled and classified by {its} angle-resolved kinetic energy release (KER) spectra.We demonstrat…
The ionization energy of ortho-H$_2$ has been determined to be $E^\mathrm{o}_\mathrm{I}(\mathrm{H}_2)/(hc)=124\,357.238\,062(25)$ cm$^{-1}$ from measurements of the GK(1,1)--X(0,1) interval by Doppler-free two-photon spectroscopy using a narrow band 179-nm laser source and the ionization energy of the GK(1,1) state by continuous-wave near-infrared laser spectroscopy. $E^\mathrm{o}_\mathrm{I}$(H$_2$) was used to derive the dissociation energy of H$_2$, $D^{N=1}_{0}$(H$_2$), at $35\,999.582\,894(25)$ cm$^{-1}$ with a precision that is more than one order of magnitude better than all previous res…
The pulsed-field-ionization zero-kinetic-energy photoelectron spectrum of H$_2$ has been recorded in the vicinity of the dissociative-ionization threshold following three-photon excitation via selected rotational levels of the B $^1Σ_u^+$ ($v=19$) and $\bar{\rm H}$ $^1Σ_g^+$ ($v=11$) intermediate states. The spectra consist of transitions to bound levels of the X$^+$ $^2Σ_g^+$ state of H$_2^+$ with $v^+$ in the range 14-19 and $N^+$ in the range 0-9, of the A$^+$ $^2Σ_u^+$ state with $v^+=0$ and $N^+=0-2$, and of shape resonances corresponding to the X$^+\ (v^+=17,N^+=7)$ and X$^+\ (v^+=18,N^+…
We present experimental results on the ionization/dissociation of methane in femtosecond pulses of radiation. Angular and intensity dependent yields of singly and doubly charged species were measured using an imaging mass spectrometer. The measured data shows that all fragments yields exhibit some degree of anisotropy as a result of them being preferably ejected parallel to the polarization direction. Additionally, an anomalous perpendicular fragmentation pattern is found for CH\-(2)\+(2+). We find evidence of multiple dissociation mechanisms including statistical decay, field assisted dissoci…
Observation of Above-Threshold Dissociation of Na$_2^+$ in Intense Laser Fields
本文报道了多电子分子Na $_2^+$的阈上解离现象。这个过程是由于在一个场修饰的分子连续谱的连续-连续跃迁。已检测到三个具有不同动能释放模式的良好分辨的碎片化通道，其中两个与通过光诱导电位的普通光解离成Na（3s）+ Na $^+$和Na（3 p）+ Na $^+$相关，一个与连续-连续跃迁和高于阈值的解离成Na（3 p）+ Na $^+$相关。我们发现，当我们穿着这个分子与一个字段的强度为~3 × 10 $^{12}$ W/cm $^2$，高于阈值的解离优于其他过程，如场电离，然后库仑爆炸。
We investigate the role of nuclear motion and strong-field-induced electronic couplings during the double ionization of deuterated water using momentum-resolved coincidence spectroscopy. By examining the three-body dicationic dissociation channel, D$^{+}$/D$^{+}$/O, for both few- and multi-cycle laser pulses, strong evidence for intra-pulse dynamics is observed. The extracted angle- and energy-resolved double ionization yields are compared to classical trajectory simulations of the dissociation dynamics occurring from different electronic states of the dication. In contrast with measurements o…
University of Gothenburg（哥德堡大学）；Université Gustave Eiffel（古斯塔夫·埃菲尔大学）；MAX IV Laboratory, Lund University（隆德大学马克四实验室）；University of Southampton（南安普顿大学）；Oxford University（牛津大学）
We experimentally and theoretically investigated the deprotonation process on nanosecond to microsecond timescale in ethylene and acetylene molecules, following their double ionization by a strong femtosecond laser field. In our experiments we utilized coincidence detection with the reaction microscope technique, and found that both the lifetime of the long-lived ethylene dication leading to the delayed deprotonation and the relative channel strength of the delayed deprotonation compared to the prompt one have no evident dependence on the laser pulse duration and the laser peak intensity. Quan…
X-ray Transient Absorption Spectroscopy (XTAS) and theoretical calculations are used to study CCl$_4^+$ prepared by 800 nm strong-field ionization. XTAS simultaneously probes atoms at the carbon K-edge (280-300 eV) and chlorine L-edge (195-220 eV). Comparison of experiment to X-ray spectra computed by orbital-optimized density functional theory (OO-DFT) indicates that after ionization, CCl$_4^+$ undergoes symmetry breaking driven by Jahn-Teller distortion away from the initial tetrahedral structure (T$_d$) in 6$\pm$2 fs. The resultant symmetry-broken covalently bonded form subsequently separat…
We present a full quantal study on the dissociation of a weakly bound molecular ion in the presence of an external time-dependent electric field. We focus on the dissociation dynamics of a molecular ion in a Paul trap relevant for atom-ion hybrid traps. Our results show that a weakly bound molecular ion survives in a Paul trap giving a theoretical ground to previous experimental findings [A. Krükow et al. Phys. Rev. Lett. 116, 193201 (2016) and A. Mohammadi et al. Phys. Rev. Research 3, 013196 (2021)]. In particular, we find that weakly bound molecular ions are more likely to survive in traps …
The laser-induced fragmentation dynamics of this most fundamental polar molecule HeH$^+$ are measured using an ion beam of helium hydride and an isotopologue at various wavelengths and intensities. In contrast to the prevailing interpretation of strong-field fragmentation, in which stretching of the molecule results primarily from laser-induced electronic excitation, experiment and theory for nonionizing dissociation, single ionization and double ionization both show that the direct vibrational excitation plays the decisive role here. We are able to reconstruct fragmentation pathways and deter…
D$_2$ molecules, excited by linearly cross-polarized femtosecond extreme ultraviolet (XUV) and near-infrared (NIR) light pulses, reveal highly structured D$^+$ ion fragment momenta and angular distributions that originate from two different 4-step dissociative ionization pathways after four photon absorption (1 XUV + 3 NIR). We show that, even for very low dissociation kinetic energy release $\le$~240~meV, specific electronic excitation pathways can be identified and isolated in the final ion momentum distributions. With the aid of {\it ab initio} electronic structure and time-dependent Schröd…
We report the production of highly spin-polarized Deuterium atoms via photodissociation of deuterium iodide at 270 nm. The velocity distribution of both the deuterium and iodine photodissociation products is performed via velocity mapping slice-imaging. Additionally, the angular momentum polarization of the iodine products is studied using polarization-sensitive ionization schemes. The results are consistent with excitation of the $A^1Π_1$ state followed by adiabatic dissociation. The process produces $\sim$100\% electronically polarized deuterium atoms at the time of dissociation, which is th…
Monosubstituted nitrotoluenes serve as important model compounds for nitroaromatic energetic molecules such as trinitrotoluene. This work investigates the ultrafast nuclear dynamics of 3- and 4-nitrotoluene radical cations using femtosecond pump-probe measurements and the results of density functional theory calculations. Strong-field adiabatic ionization of 3- and 4-nitrotoluene using 1500 nm, 18 fs pulses produces radical cations in the ground electronic state with distinct coherent vibrational excitations. In both nitrotoluene isomers, a one-photon excitation with the probe pulse results in…
This paper provides new insights concerning the simulation of plasmon driven chemical reactions using real-time TDDFT based on the tight-binding electronic structure code DFTB+, with applications to the dissociation of H$_2$ on octahedral silver and gold nanoparticles with 19-489 atoms. A new component of these calculations involves sampling a 300 K canonical ensemble to determine the distribution of possible outcomes of the calculations, and with this approach we are able to determine the threshold for dissociation as a function of laser intensity, wavelength, and nanocluster size. We show th…
Adsorption and dissociation of hydrocarbons on metallic surfaces represent crucial steps to carburization of metal. Here, we use density functional theory total energy calculations with the climbing-image nudged elastic band method to estimate the adsorption energies and dissociation barriers for different CO coverages with surface supercells of different sizes. For the absorption of CO, the contribution from van der Waals interaction in the computation of adsorption parameters is found important in small systems with high CO-coverages. The dissociation process involves carbon insertion into t…
We report measurements on the H$^{+}$ + H$^{+}$ fragmentation channel following direct single-photon double ionization of neutral NH$_{3}$ at 61.5 eV, where the two photoelectrons and two protons are measured in coincidence using 3-D momentum imaging. We identify four dication electronic states that contribute to H$^{+}$ + H$^{+}$ dissociation, based on our multireference configuration-interaction calculations of the dication potential energy surfaces. The extracted branching ratios between these four dication electronic states are presented. Of the four dication electronic states, three disso…
Current Non-Orthogonal Configuration Interaction (NOCI) methods often use a set of Self-Consistent Field (SCF) states selected based on chemical intuition. However, it may be challenging to track these SCF states across a dissociation profile and the NOCI states recovered may be spin contaminated. In this paper, we propose a method of applying spin rotation on symmetry broken UHF (sb-UHF) states to generate a basis for NOCI. The dissociation of ethene was examined by localising spin rotation on each resulting carbene fragment. We show that this gives a size-consistent description of its dissoc…
Photo-ionization induced ultrafast electron dynamics is considered as a precursor to the slower nuclear dynamics associated with molecular dissociation. Here, using ab initio multielectron wave-packet propagation method, we study the overall many-electron dynamics, triggered by the ionization of outer-valence orbitals of different tautomers of a prototype molecule with more than one symmetry element. From the time evolution of the initially created averaged hole density of each system, we identify distinctly different charge dynamics response in the tautomers. We observe that keto form shows c…
Laser pulses with stable electric field waveforms establish the opportunity to achieve coherent control on attosecond timescales. We present experimental and theoretical results on the steering of electronic motion in a multi-electron system. A very high degree of light-waveform control over the directional emission of C+ and O+ fragments from the dissociative ionization of CO was observed. Ab initio based model calculations reveal contributions to the control related to the ionization and laser-induced population transfer between excited electronic states of CO+ during dissociation.
The specific role played by small gold nanoparticles supported on the rutile TiO2(110) surface in the processes of adsorption and dissociation of H2 is discussed. It is demonstrated that the molecular and dissociative adsorption of H2 on Au_n clusters containing n = 1, 2, 8 and 20 atoms depends on cluster size, geometry structure, cluster flexibility and the interaction with the support material. Rutile TiO2(110) support energetically promotes H2 dissociation on gold clusters. It is demonstrated that the active sites towards H2 dissociation are located at corners and edges on the surface of th…
Many chemical reactions involve bond-dissociation. This is also true for reactions at solid surfaces, in which the dissociation step is often limiting but facilitated in comparison to gas phase reaction channels. This work considers hydrogen dissociation. Reliable molecular beam results are available for this reaction at some copper surfaces. Heterogeneous catalysis by copper is simulated. It was investigated in our previous work since it is in many ways a prototype metal presenting a close-packed surface here. These hydrogen molecules are adsorbed at Cu(111) and fixed geometries on the dissoc…
We report the first experimental measurement of the near-threshold photo-ionization spectra of polycyclic aromatic hydrocarbon clusters made of pyrene C16H10 and coronene C24H12, obtained using imaging photoelectron photoion coincidence spectrometry with a VUV synchrotron beamline. The experimental results of the ionization energy are confronted to calculated ones obtained from simulations using dedicated electronic structure treatment for large ionized molecular clusters. Experiment and theory consistently find a decrease of the ionization energy with cluster size. The inclusion of temperatur…
The method of increments (MoI) allows one to successfully calculate cohesive energies of bulk materials with high accuracy, but it encounters difficulties when calculating whole dissociation curves. The reason is that its standard formalism is based on a single Hartree-Fock (HF) configuration whose orbitals are localized and used for the many-body expansion. Therefore, in those situations where HF does not allow a size-consistent description of the dissociation, the MoI cannot yield proper results either. Herein we address the problem by employing a size-consistent multiconfigurational referen…
Kinetic isotope effects (KIEs) taking place in mass spectrometry (MS) can provide in-depth insights into the fragmental behaviors of compounds in MS. Yet the mechanisms of KIEs in collision-induced dissociation (CID) in tandem MS are unclear, and information about chlorine KIEs (Cl-KIEs) of organochlorines in MS is particularly scarce. This study investigated the Cl-KIEs of dichloromethane, trichloroethylene and tetrachloroethylene during CID using gas chromatography-electron ionization triple-quadrupole tandem MS. Cl-KIEs were measured with MS signal intensities, and their validity was confir…
