Photoionization Dynamics Research Articles

VUV photoionization dynamics of the C60 buckminsterfullerene: 2D-matrix photoelectron spectroscopy in an astrophysical context.

We present the photoionization dynamics of the C60 buckminsterfullerene from threshold up to 14.0 eV recorded with VUV synchrotron radiation at the DESIRS beamline at the SOLEIL synchrotron. The recorded data is obtained using a double-imaging photoelectron photoion coincidence spectrometer and is presented as a two-dimensional photoelectron matrix which contains a wealth of spectroscopic data. We present these data in an astrophysical context which relates to (i) the threshold photoelectron spectrum which is compared to data relevant to the diffuse interstellar bands (DIBs), (ii) the kinetic photoelectron distribution at the Lyman-α line which is relevant to the dominant heating source in the ISM, and (iii) the absolute photoionization cross section of C60 up to approx. 10.5 eV. The photoelectron spectrum implies that the symmetry of the ground state is different than previous theoretical models have predicted, and this result is discussed in context of recent experimental and theoretical findings. Also presented are partial photoionization cross sections of the first two photoelectron bands and their anisotropy parameters. These data are compared with previous theoretical values and discussed where appropriate.

Determination of the Interaction Potential and Rovibrational Structure of the Ground Electronic State of MgAr+ Using PFI-ZEKE Photoelectron Spectroscopy

The interaction potential characterizing the ground electronic state of MgAr+ has been determined from the photoelectron spectrum recorded from the a 3Π0 metastable state of MgAr at high resolution by pulsed-field-ionization zero-kinetic-energy (PFI-ZEKE) photoelectron spectroscopy. The photoelectron spectrum provides information on the first ten vibrational levels of MgAr+ and leads to the determination of the adiabatic ionization energy of metastable MgAr (38 742.3(20) cm-1), the ground state dissociation energy of MgAr+ (1254(60) cm-1), and to the characterization of the rovibrational photoionization dynamics of MgAr.

Dissociative photoionization of NO across a shape resonance in the XUV range using circularly polarized synchrotron radiation.

We report benchmark results for dissociative photoionization (DPI) spectroscopy and dynamics of the NO molecule in the region of the σ* shape resonance in the ionization leading to the NO+(c3Π) ionic state. The experimental study combines well characterized extreme ultraviolet (XUV) circularly polarized synchrotron radiation, delivered at the DESIRS beamline (SOLEIL), with ion-electron coincidence 3D momentum spectroscopy. The measured (N+, e) kinetic energy correlation diagrams reported at four discrete photon energies in the extended 23-33 eV energy range allow for resolving the different active DPI reactions and underline the importance of spectrally resolved studies using synchrotron radiation in the context of time-resolved studies where photoionization is induced by broadband XUV attosecond pulses. In the dominant DPI reaction which leads to the NO+(c3Π) ionic state, photoionization dynamics across the σ* shape resonance are probed by molecular frame photoelectron angular distributions where the parallel and perpendicular transitions are highlighted, as well as the circular dichroism CDAD(θe) in the molecular frame. The latter also constitute benchmark references for molecular polarimetry. The measured dynamical parameters are well described by multichannel Schwinger configuration interaction calculations. Similar results are obtained for the DPI spectroscopy of highly excited NO+ electronic states populated in the explored XUV photon energy range.

Photoionization dynamics of endohedrally confined atomic H and Ar: a contrasting study between compact versus diffused model potential

Photoionization from H@C60 and Ar@C60 is studied by employing two different model potentials to simulate the endohedral environment. The contrast between the diffusive Gaussian annular square well (GASW) and the compact annular square well (ASW) model potential on the photoionization dynamics is explored by studying the cross-section, phase shift, and Wigner time delay. A realistic description of the fullerene environment requires the right amount of diffuseness and compactness, and the proposed GASW model has both of these attributes. The dynamical properties of an encapsulated atom are studied systematically as a function of the well depth, and it is found that the GASW model induces mild and realistic confinement oscillations on the photoionization parameters in comparison with the ASW case. In addition, the present work brings out a few other interesting features. For a confining well depth of 1.03 a.u., the phase of the dipole matrix elements takes sharp jumps akin to the behavior of dipole phases at the Cooper minimum. In the case of free Ar, the correlation effects contribute less to the time delay in comparison with screening effects near the Cooper minimum. In search of a realistic potential to mimic confinement, the GASW model potential is recommended.

Spatio-temporal measurement of ionization-induced modal index changes in gas-filled PCF by prism-assisted side-coupling.

We report the use of prism-assisted side-coupling to investigate the spatio-temporal dynamics of photoionization in an Ar-filled hollow-core photonic crystal fiber. By launching four different LP core modes we are able to probe temporal and spatial changes in the modal refractive index on timescales from a few hundred picoseconds to several hundred microseconds after the ionization event. We experimentally analyze the underlying gas density waves and find good agreement with quantitative and qualitative hydrodynamic predictions. Moreover, we observe periodic modulations in the MHz-range lasting for a few microseconds, indicating nanometer-scale vibrations of the fiber structure, driven by gas density waves.

To Be or Not To Be a Molecular Ion: The Role of the Solvent in Photoionization of Arginine.

Application of photoionization mass spectroscopy, a technique capable of assessing protonation states in complex molecules in the gas phase, is challenging for arginine due to its fragility. We report photoionization efficiencies in the valence region of aqueous aerosol particles produced from arginine solutions under various pH and vaporization conditions. By using ab initio calculations, we investigate the stability of different conformers. Our results show that neutral arginine fragments upon ionization in the gas phase but solvation stabilizes the molecular ion, resulting in different photoionization dynamics. We also report the valence-band photoelectron spectra of the aerosol solutions obtained at different pH values.

Effects of core space and excitation levels on ground-state correlation and photoionization dynamics of Be and Ne.

We explore the effects of correlation on the ground-state energies and on photoionization dynamics in atomic Be and Ne. We apply the time-dependent restricted-active-space self-consistent-field method for several excitation schemes and active orbital spaces with and without a dynamic core to address the effects systematically at different levels of approximation. For the ground-state many-electron wave functions, we compare the correlation energies with entropic measures of entanglement. A larger magnitude of the correlation energy does not always correspond to a larger value of the considered entanglement measures. To evaluate the impact of correlation in a process involving continua, we consider photoionization by attosecond pulses. The photoelectron spectra may be significantly affected by including a dynamical core.

The photoionization dynamics based on molecular pre-orientation.

We study theoretically the photoionization dynamics of pre-oriented NaK molecule. Firstly, a THz laser pulse is utilized to orient the ground state molecule. And then the pump and probe laser pulses are used to excite and ionize the molecule, respectively. We study the influence of molecular orientation duration and degree on the ionization probability, angle-resolved photoelectron spectrum and photoelectron angular distribution (PAD). It is shown that we could obtain more stable ionization signal and PAD when the molecules are ionized in molecular orientation duration. We could increase the ionization probability and obtain more concentrated ionization signal and photoelectron distribution by increasing the orientation degree in the ground state. Moreover, we discuss the splitting pattern in the angle-resolved photoelectron spectrum.

Direct observation of photoionization dynamics in solution phase induced by femtosecond two-photon excitation

In solution phase, the solute can be photo-ionized in the lower excitation energy than its ionization potential in gas phase. Therefore, the specific interaction is expected to be exist between the surrounding media and higher excited (Sn) state of the solute. In order to elucidate such polarization effect of solvent on the photoionization process, femtosecond double-pulse excitation was applied to direct detection of low-energy photoionization dynamics of a phenylenediamine derivative in solution phase. From the results of the transient absorption change, in polar solvent, it is clearly indicated that photoionization does not proceed directly from the Sn state, but through specific intermediate state. Moreover,

Ionization dynamics of a phenylenediamine derivative in solutions as revealed by femtosecond simultaneous and stepwise two-photon excitation.

Femtosecond transient absorption spectroscopy with off-resonant simultaneous and resonant stepwise two-photon excitation methods were applied to the direct observation of photoionization dynamics of a phenylenediamine derivative in n-hexane, ethanol and acetonitrile solutions. Upon the selective excitation of the solute via the off-resonant two-photon excitation to the energy level almost equivalent with the ionization potential in the gas phase, rapid appearance of the radical cation (within ca. 100-200 fs) was observed in polar and nonpolar solutions. On the other hand, in the case where the excited energy level from the ground state is 0.8 eV lower than the ionization potential in the gas phase, the radical cation appears only in polar solutions in sub-ps to ps time scales, indicating that the photoionization does not occur directly from the highly electronically excited state even in the polar solution. Comparison of the dynamics between ethanol and acetonitrile solutions strongly suggested that the solvation process of the precursor species leading to the ionization took a crucial role in the electron ejection process with lower energy in polar solutions.

Ultrafast imaging of laser-controlled non-adiabatic dynamics in NO2 from time-resolved photoelectron emission.

Time-resolving and controlling coupled electronic and nuclear dynamics at conical intersections on the sub-femtosecond to few-femtosecond time scale is among the challenging goals of attosecond physics. Here we present numerical simulations of time-resolved photoelectron spectroscopy of such dynamics in NO2, where the coupled electron-nuclear motion at the 2A1/2B2 conical intersection is steered on the sub-laser-cycle time scale by a nearly single-cycle, waveform controlled mid-infrared laser pulse. For a rigorous description of the photoionization dynamics, we employ ab initio energy- and geometry-resolved photoionization matrix elements obtained with the multichannel R-matrix method, using a multiconfigurational description of the molecule and a newly developed algorithm to generate photoionization dipoles that are phase consistent on the level of both the neutral and the ionic states. We find that for sufficient molecular alignment, the time- and energy-resolved anisotropy parameters of the photoelectron angular distributions provide a particularly clear picture of both the ultrafast natural molecular dynamics at the conical intersection and its modifications by the control pulse. In particular, changes in the electronic and nuclear configurations induced by the control pulse lead to the appearance of non-vanishing odd anisotropy parameters in the photoelectron spectra. These are absent in the spectra obtained without the control pulse and therefore provide sensitive, background-free diagnostic of the control.

Electronic wavefunctions probed by all-optical attosecond interferometry

Photoelectron spectroscopy is a powerful method that provides insight into the quantum mechanical properties of a wide range of systems. The ionized electron wavefunction carries information on the structure of the bound orbital, the ionic potential as well as the photo-ionization dynamics itself. While photoelectron spectroscopy resolves the absolute amplitude of the wavefunction, retrieving the spectral phase information has been a long-standing challenge. Here, we transfer the electron phase retrieval problem into an optical one by measuring the time-reversed process of photo-ionization -- photo-recombination -- in attosecond pulse generation. We demonstrate all-optical interferometry of two independent phase-locked attosecond light sources. This measurement enables us to directly determine the phase shift associated with electron scattering in simple quantum systems such as helium and neon, over a large energy range. In addition, the strong-field nature of attosecond pulse generation resolves the dipole phase around the Cooper minimum in argon through a single scattering angle, along with phase signatures of multi-electron effects. Our study bears the prospect of probing complex orbital phases in molecular systems as well as electron correlations through resonances subject to strong laser fields.

Photoionization dynamics of cis-dichloroethene from investigation of vibrationally resolved photoelectron spectra and angular distributions.

The influence of vibronic coupling on the outer valence ionic states of cis-dichloroethene has been investigated by recording photoelectron spectra over the excitation range 19-90 eV using plane polarized synchrotron radiation, for two polarization orientations. The photoelectron anisotropy parameters and electronic state branching ratios derived from these spectra have been compared to theoretical predictions obtained with the continuum multiple scattering approach. This comparison shows that the photoionization dynamics of the 2B2, 2A1, 2A2, and 2B1 states, all of which are formed through the ejection of an electron from a nominally chlorine lone-pair orbital, exhibit distinct evidence of the Cooper minimum associated with the halogen atom. While retaining a high degree of atomic character, these orbital ionizations nevertheless display clear distinctions. Simulations, assuming the validity of the Born-Oppenheimer and the Franck-Condon approximations, of the 2B1, 2B2, and 2B1 state photoelectron bands have allowed some of the vibrational structure observed in the experimental spectra to be assigned. The simulations provide a very satisfactory interpretation for the 2B1 state band but appear less successful for the 2B2 and 2B1 states, with irregularities appearing in both. The 2A1 and 2A2 state photoelectron bands exhibit very diffuse and erratic profiles that cannot be reproduced at this level. Photoelectron anisotropy parameters, β, have been evaluated as a function of binding energy across the studied photon energy range. There is a clear step change in the β values of the 2B2 band at the onset of the perturbed peak intensities, with β evidently adopting the value of the 2A1 band β. The 2B1 band β values also display an unexpected vibrational level dependence, contradicting Franck-Condon expectations. These various behaviors are inferred to be a consequence of vibronic coupling in this system.

Orientation-dependent stereo Wigner time delay and electron localization in a small molecule.

Attosecond metrology of atoms has accessed the time scale of the most fundamental processes in quantum mechanics. Transferring the time-resolved photoelectric effect from atoms to molecules considerably increases experimental and theoretical challenges. Here we show that orientation- and energy-resolved measurements characterize the molecular stereo Wigner time delay. This observable provides direct information on the localization of the excited electron wave packet within the molecular potential. Furthermore, we demonstrate that photoelectrons resulting from the dissociative ionization process of the CO molecule are preferentially emitted from the carbon end for dissociative 2Σ states and from the center and oxygen end for the 2Π states of the molecular ion. Supported by comprehensive theoretical calculations, this work constitutes a complete spatially and temporally resolved reconstruction of the molecular photoelectric effect.

Time and place of electron exit

Attosecond Dynamics Until about a decade ago, laser-induced ionization was considered instantaneous. Since then, applications of attosecond laser pulses have shown multiple subtle and complex factors that influence the precise timing of electron ejection from atoms and surfaces. Vos et al. measured the corresponding attosecond dynamics of dissociative photoionization in a diatomic molecule, carbon monoxide. By imaging the charged fragments, the timing could be correlated with the specific spatial portion of the molecule from which the electron wave packet emerged. Science , this issue p. [1326][1] [1]: /lookup/doi/10.1126/science.aao4731

Ab initio photodynamics of model EUV photoresists

Tin-oxo cages belong to a class of organometallic compounds which were recently recognized as promising photoresist materials for the extreme ultraviolet (EUV) lithography – a method proposed for the new generation of integrated circuits. The EUV exposure of tin-oxo cages causes significant structural changes; however, the molecular mechanism of these changes is to a large extent unknown. In the present work, we focus on the photoionization dynamics of the small tin-oxo molecules: the trimethlytin hydroxide (TMTH) and trihydroxymethyl stannane (THMS) molecules. We employed the surface hopping (SH) dynamics on the Floating Occupation Molecular Orbital Complete Active Space Configuration Interaction (FOMO-CASCI) potential energy surfaces accelerated with graphical processor units (GPU). After the ionization of both molecules, we observed an ultrafast relaxation (∼100 fs) into the ground and first excited electronic states followed by a rapid dissociation yielding the neutral CH3 and OH radicals and a charged remainder. However, the dissociation dynamic does not occur solely on the hot ground electronic state and reaction outcome partially depends on initially ionized state. Our work also demonstrate that the SH+FOMO-CASSCI based dynamics is suitable for electron-rich open-shell systems.

On-Demand Generation of Neutral and Negatively Charged Silicon-Vacancy Centers in Diamond.

Point defects in wide-band-gap semiconductors are emerging as versatile resources for nanoscale sensing and quantum information science, but our understanding of the photoionization dynamics is presently incomplete. Here, we use two-color confocal microscopy to investigate the dynamics of charge in type 1b diamond hosting nitrogen-vacancy (NV) and silicon-vacancy (SiV) centers. By examining the nonlocal fluorescence patterns emerging from local laser excitation, we show that, in the simultaneous presence of photogenerated electrons and holes, SiV (NV) centers selectively transform into the negative (neutral) charge state. Unlike NVs, 532nm illumination ionizes SiV^{-} via a single-photon process, thus hinting at a comparatively shallower ground state. In particular, slower ionization rates at longer wavelengths suggest the latter lies approximately ∼1.9 eV below the conduction band minimum. Building on the above observations, we demonstrate on-demand SiV and NV charge initialization over large areas via green laser illumination of variable intensity.

Attosecond photoionization dynamics in neon

We study the role of electron-electron correlation in the ground-state of Ne, as well as in photoionization dynamics induced by an attosecond XUV pulse. For a selection of central photon energies around 100 eV, we find that while the mean-field time-dependent Hartree-Fock method provides qualitatively correct results for the total ionization yield, the photoionization cross section, the photoelectron momentum distribution as well as for the time-delay in photoionization, electron-electron correlation is important for a quantitative description of these quantities.

Extracting attosecond delays from spectrally overlapping interferograms

Attosecond interferometry is becoming an increasingly popular technique for measuring the dynamics of photoionization in real time. Whereas early measurements focused on atomic systems with very simple photoelectron spectra, the technique is now being applied to more complex systems including isolated molecules and solids. The increase in complexity translates into an augmented spectral congestion, unavoidably resulting in spectral overlap in attosecond interferograms. Here, we discuss currently used methods for phase retrieval and introduce two new approaches for determining attosecond photoemission delays from spectrally overlapping photoelectron spectra. We show that the previously used technique, consisting in the spectral integration of the areas of interest, does in general not provide reliable results. Our methods resolve this problem, thereby opening the technique of attosecond interferometry to complex systems and fully exploiting its specific advantages in terms of spectral resolution compared to attosecond streaking.

Temporal interference driven by an oscillating electric field in photodetachment of H− ion**Project supported by the National Natural Science Foundation of China (Grant No. 11374133) and the Taishan Scholars Project of Shandong Province, China (Grant No. ts2015110055).

The real time domain interferometry for the photodetachment dynamics driven by the oscillating electric field has been studied for the first time. Both the geometry of the detached electron trajectories and the electron probability density are shown to be different from those in the photodetachment dynamics in a static electric field. The influence of the oscillating electric field on the detached electron leads to a surprisingly intricate shape of the electron waves, and multiple interfering trajectories generate complex interference patterns in the electron probability density. Using the semiclassical open-orbit theory, we calculate the interference patterns in the time-dependent electron probability density for different electric field strengths, different frequencies and phases in the oscillating electric field. This method is universal, and can be extended to study the photoionization dynamics of the atoms in the time-dependent electric field. Our study can guide the future experimental researches in the photodetachment or photoionization microscopy of negative ions and atoms in the oscillating electric field.