The role of Rydberg states in photoionization of NO2 and (NO+, O-) ion pair formation induced by one VUV photon.

We report a combined experimental and theoretical study of photoionization (PI) of the NO2 molecule into the NO2(+) (X (1)Σg(+)) ground state and the photodissociation of NO2 into the NO(+)((1)Σ(+)) + O(-)((2)P) ion pair. These processes were induced by 10.9 eV-13 eV synchrotron radiation and the products were detected using electron-ion or O(-)-NO(+) coincident momentum spectroscopy. The results demonstrate the strong influence of [R(∗)(4b2)(-1), nlα(i), v2(')] Rydberg states vibrationally resolved in the v2(') bending modes for both processes. In particular, we emphasize two regions around 11.5 eV and 12.5 eV that were studied in more detail for their relevance to 400 nm multiphoton ionization induced by femtosecond pulses. The photoelectron energy spectra and asymmetry parameters support the existence of two PI mechanisms, as probed with the help of fixed-nuclei frozen-core Hartree-Fock calculations. We found significant deviations from Franck-Condon ionization predictions which may be assigned to vibronic coupling of NO2(∗) states such as that induced by a conical intersection. The limited agreement between theory and experiment, even for the non-resonant processes, indicates the need for calculations that go beyond the approximations used in the current study. Ion pair formation leads to strong vibrational and rotational excitation of the NO(+)((1)Σ(+),v) product, with an ion fragment angular anisotropy depending on both the v2(') bending quantum number of the excited parent molecule and the v vibrational level of the fragment.

Circular dichroism in photoionization of H2.

Circular dichroism is a consequence of chirality. However, nonchiral molecules can also exhibit it when the measurement itself introduces chirality, e.g., when measuring molecular-frame photoelectron angular distributions. The few such experiments performed on homonuclear diatomic molecules show that, as expected, circular dichroism vanishes when the molecular-frame photoelectron angular distributions are integrated over the polar electron emission angle. Here we show that this is not the case in resonant dissociative ionization of H2 for photons of 30-35 eV, which is the consequence of the delayed ionization from molecular doubly excited states into ionic states of different inversion symmetry.

Ion pair formation in multiphoton excitation of NO(2) using linearly and circularly polarized femtosecond light pulses: kinetic energy distribution and fragment recoil anisotropy.

The NO(2) ion pair photodissociation dynamics leading to NO(+)(X(1)Sigma(+),v) + O(-)((2)P(3/2) or (2)P(1/2)), induced by a 1 kHz femtosecond laser with wavelengths near 400 nm, has been characterized using the coincidence vector correlation method. The ion pair production after four-photon absorption reaches more than 15% of the primary ionization. The kinetic energy release of the fragments demonstrates a significant vibrational excitation of the NO(+)(X(1)Sigma(+),v) molecular fragment. Recoil ion fragment emission is strongly aligned along the polarization axis of linearly polarized light or preferentially emitted in the plane perpendicular to the propagation axis of circularly polarized light. The formalism describing the recoil anisotropy for bound-to-bound n-photon transition inducing prompt axial recoil dissociation of a nonlinear molecule has been developed to interpret the measured anisotropies in terms of excitation pathways via near-resonant intermediate states of specific symmetries. Possible reaction pathways are discussed that are consistent with the data and supported by calculations of potential energy surfaces and transition moments.

Photodissociation dynamics of Ar2(+) and Ar3(+) excited by 527 nm photons.

The photofragmentation dynamics of Ar(2)(+) and Ar(3)(+) clusters has been investigated at a 527 nm wavelength (2.35 eV) using a setup that allows simultaneous detection of the ionic and neutral fragments in a coincidence experiment. Measurement of positions and times of flight enables in principle a complete description of the fragmentation dynamics. The photofragmentation dynamics of Ar(3)(+) clusters is similar to that of Ar(2)(+) with, in addition, the ejection of a third fragment that can be neutral or ionized via a resonant electron capture. This is attributed to the triangular geometry of the Ar(3)(+) ion.

A zero dead-time multi-particle time and position sensitive detector based on correlation between brightness and amplitude.

A new multi-particle time and position sensitive detector using only a set of microchannel plates, a waveform digitizer, a phosphor screen, and a CMOS camera is described. The assignment of the timing information, as taken from the microchannel plates by fast digitizing, to the positions, as recorded by the camera, is based on the COrrelation between the BRightness of the phosphor screen spots, defined as their integrated intensity and the Amplitude of the electrical signals (COBRA). Tests performed by observing the dissociation of HeH, the fragmentation of H3 into two or three fragments, and the photo-double-ionization of Xenon atoms are presented, which illustrate the performances of the COBRA detection scheme.

Flexible attosecond beamline for high harmonic spectroscopy and XUV/near-IR pump probe experiments requiring long acquisition times.

We describe the versatile features of the attosecond beamline recently installed at CEA-Saclay on the PLFA kHz laser. It combines a fine and very complete set of diagnostics enabling high harmonic spectroscopy (HHS) through the advanced characterization of the amplitude, phase, and polarization of the harmonic emission. It also allows a variety of photo-ionization experiments using magnetic bottle and COLTRIMS (COLd Target Recoil Ion Momentum Microscopy) electron spectrometers that may be used simultaneously, thanks to a two-foci configuration. Using both passive and active stabilization, special care was paid to the long term stability of the system to allow, using both experimental approaches, time resolved studies with attosecond precision, typically over several hours of acquisition times. As an illustration, applications to multi-orbital HHS and electron-ion coincidence time resolved spectroscopy are presented.

Influence of gold coating and interplate voltage on the performance of chevron micro-channel plates for temporally and spatially resolved single particle detection.

We present a study of two different sets of Micro-Channel Plates used for time and space resolved single particle detection. We investigate the effects of the gold coating and that of introducing an interplate voltage between the spatially separated plates. We find that the gold coating increases the count rate of the detector and the pulse amplitude as previously reported for non-spatially resolved setups. The interplate voltage also increases count rates. In addition, we find that a non-zero interplate voltage improves the spatial accuracy in determining the arrival position of incoming single particles (by ~20%) while the gold coating has a negative effect (by ~30%).

Characterization of neutral fragments issued from the photodissociation of protonated tryptophane.

New information on the photo-fragmentation of biomolecules is obtained from the detection of neutral and ionic fragments using a time and position resolved coincidence technique that reveals whether an ionic photofragment is associated with one or more neutral fragments. In the case of a sequential dissociation, both fragmentation channels are identified as well as their time ordering.

Dissociative charge transfer and collision induced dissociation of Ar2+ and Ar3+ clusters in collisions with argon atoms at keV energies.

The dynamics of dissociative charge transfer and collision induced dissociation of Ar(2) (+) and Ar(3) (+) clusters colliding with Ar atoms at 4.8 keV has been investigated using a novel multifragment detection scheme that maps the postcollision vectors of all particles simultaneously. Estimation of internal energies and measurement of pre- and postcollision vectors enables a full description of reaction dynamics. The prominence of electronic excitation in defining the dynamics of these collision systems is demonstrated. The dissociation dynamics of Ar(3) (+) clusters is distinctly different from that of Ar(2) (+). This is attributed to a combination of lower internal energies and predominantly triangular T-shape structure of the Ar(3) (+) ion.

Lifetime and yield of metastable Ar2(+) ions.

Ar2(+) ions produced in a cooled supersonic expansion by electron-impact ionization are accelerated at 2.5 keV and kept during few milliseconds inside a linear electrostatic trap. The lifetime of the metastable Ar2(+) ion is determined from the measurement of the rate of the argon atoms escaping the trap. The lifetime and the relative metastable populations are measured as a function of the pressure and temperature in the supersonic expansion, i.e., of the mean cluster size. Possible mechanisms responsible for the metastable formation are discussed.