ORCID Profile
0000-0002-7200-3775
Current Organisation
E O Lawrence Berkeley National Laboratory
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Publisher: Royal Society of Chemistry (RSC)
Date: 2020
DOI: 10.1039/D0CP01522A
Abstract: 3D momentum imaging investigation of the dynamics of dissociative electron attachment to formic acid, producing a hydride anion and either formyloxyl or hydrocarboxyl radicals.
Publisher: AIP Publishing
Date: 14-07-2020
DOI: 10.1063/5.0013485
Abstract: We present a combined experimental and theoretical study on the photodissociation dynamics of ion-pair formation in O2 following resonant two-photon absorption of a 9.3 eV femtosecond pulse, where the resulting O+ ions are detected using 3D momentum imaging. Ion-pair formation states of Σg−3 and 3Πg symmetry are accessed through predissociation of optically dark continuum Rydberg states converging to the B Σg−2 ionic state, which are resonantly populated via a mixture of both parallel–parallel and parallel–perpendicular two-photon transitions. This mixture is evident in the angular distribution of the dissociation relative to the light polarization and varies with the kinetic energy release (KER) of the fragmenting ion pair. The KER-dependent photoion angular distribution reveals the underlying two-photon absorption dynamics involved in the ion-pair production mechanism and indicates the existence of two nearly degenerate continuum resonances possessing different symmetries, which can decay by coupling to ion-pair states of the same total symmetry through internal conversion.
Publisher: AIP Publishing
Date: 11-01-2023
DOI: 10.1063/5.0128846
Abstract: We present an experimental and theoretical energy- and angle-resolved investigation on the non-dissociative photoionization dynamics of near-resonant, one-color, two-photon, single valence ionization of neutral O2 molecules. Using 9.3 eV femtosecond pulses produced via high harmonic generation and a 3-D momentum imaging spectrometer, we detect the photoelectrons and O2+ cations produced from one-color, two-photon ionization in coincidence. The measured and calculated photoelectron angular distributions show agreement, which indicates that a superposition of two intermediate electronic states is dominantly involved and that wavepacket motion on those near-resonantly populated intermediate states does not play a significant role in the measured two-photon ionization dynamics. Here, we find greater utility in the diabatic representation compared to the adiabatic representation, where invoking a single valence-character diabat is sufficient to describe the underlying two-photon ionization mechanism.
Publisher: IOP Publishing
Date: 07-09-2015
Publisher: AIP Publishing
Date: 17-09-2014
DOI: 10.1063/1.4894853
Abstract: The absolute photoabsorption cross section of propyne was recorded between 62 000 and 88 000 cm−1 by using the vacuum-ultraviolet, Fourier-transform spectrometer at the Synchrotron Soleil. This cross section spans the region including the lowest Rydberg bands and extends above the Franck-Condon envelope for ionization to the ground electronic state of the propyne cation, $\\tilde X^ +$X̃+. Room-temperature spectra were recorded in a flowing cell at 0.9 cm−1 resolution, and jet-cooled spectra were recorded at 1.8 cm−1 resolution and a rotational temperature of ∼100 K. The reduced widths of the rotational band envelopes in the latter spectra reveal new structure and simplify a number of assignments. Although nf Rydberg series have not been assigned previously in the photoabsorption spectrum of propyne, arguments are presented for their potential importance, and the assignment of one nf series is proposed. As expected from previous photoelectron spectra, Rydberg series are also observed above the adiabatic ionization threshold that converge to the v3+ = 1 and 2 levels of the C≡C stretching vibration.
Publisher: ACM
Date: 26-07-2020
Publisher: IOP Publishing
Date: 19-11-2020
Abstract: We present state-selective measurements on the N H 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 3D momentum imaging. Three dication electronic states are identified to contribute to the N H 2 + + H + dissociation channel, where the excitation in one of the three states undergoes intersystem crossing prior to dissociation, producing a cold N H 2 + fragment. In contrast, the other two states directly dissociate, producing a ro-vibrationally excited N H 2 + fragment with roughly 1 eV of internal energy. The NH + + H + + H channel is fed by direct dissociation from three intermediate dication states, one of which is shared with the N H 2 + + H + channel. We find evidence of autoionization contributing to each of the double ionization channels. The distributions of the relative emission angle between the two photoelectrons, as well as the relative angle between the recoil axis of the molecular breakup and the polarization vector of the ionizing field, are also presented to provide insight on both the photoionization and photodissociation mechanisms for the different dication states.
Publisher: AIP Publishing
Date: 16-07-2015
DOI: 10.1063/1.4926541
Abstract: The absolute photoabsorption cross sections of 1- and 2-butyne have been recorded at high resolution by using the vacuum-ultraviolet Fourier-Transform spectrometer at the SOLEIL Synchrotron. Both spectra show more resolved structure than previously observed, especially in the case of 2-butyne. In this work, we assess the potential importance of Rydberg states with higher values of orbital angular momentum, l, than are typically observed in photoabsorption experiments from ground state molecules. We show how the character of the highest occupied molecular orbitals in 1- and 2-butyne suggests the potential importance of transitions to such high-l (l = 3 and 4) Rydberg states. Furthermore, we use theoretical calculations of the partial wave composition of the absorption cross section just above the ionization threshold and the principle of continuity of oscillator strength through an ionization threshold to support this conclusion. The new absolute photoabsorption cross sections are discussed in light of these arguments, and the results are consistent with the expectations. This type of argument should be valuable for assessing the potential importance of different Rydberg series when sufficiently accurate direct quantum chemical calculations are difficult, for ex le, in the n ≥ 5 manifolds of excited states of larger molecules.
Publisher: American Physical Society (APS)
Date: 09-10-2020
Publisher: Royal Society of Chemistry (RSC)
Date: 2018
DOI: 10.1039/C8CP03637C
Abstract: Photoionization of the 4t 2 orbital of CF 4 shows overlapping resonances close to threshold, leading to a striking inversion of the photoelectron angular distribution when viewed in the body-frame.
Publisher: AIP Publishing
Date: 05-09-2023
DOI: 10.1063/5.0159300
Publisher: American Chemical Society (ACS)
Date: 15-10-2015
Abstract: The room-temperature photoabsorption spectra of a number of linear alkynes with internal triple bonds (e.g., 2-butyne, 2-pentyne, and 2- and 3-hexyne) show similar resonances just above the lowest ionization threshold of the neutral molecules. These features result in a substantial enhancement of the photoabsorption cross sections relative to the cross sections of alkynes with terminal triple bonds (e.g., propyne, 1-butyne, 1-pentyne, ...). Based on earlier work on 2-butyne [ Xu et al., J. Chem. Phys. 2012, 136, 154303 ], these features are assigned to excitation from the neutral highest occupied molecular orbital (HOMO) to a shape resonance with g (l = 4) character and approximate π symmetry. This generic behavior results from the similarity of the HOMOs in all internal alkynes, as well as the similarity of the corresponding gπ virtual orbital in the continuum. Theoretical calculations of the absorption spectrum above the ionization threshold for the 2- and 3-alkynes show the presence of a shape resonance when the coupling between the two degenerate or nearly degenerate π channels is included, with a dominant contribution from l = 4. These calculations thus confirm the qualitative arguments for the importance of the l = 4 continuum near threshold for internal alkynes, which should also apply to other linear internal alkynes and alkynyl radicals. The 1-alkynes do not have such high partial waves present in the shape resonance. The lower l partial waves in these systems are consistent with the broader features observed in the corresponding spectra.
Publisher: Springer Science and Business Media LLC
Date: 09-2022
DOI: 10.1038/S41467-022-32836-6
Abstract: The double photoionization of a molecule by one photon ejects two electrons and typically creates an unstable dication. Observing the subsequent fragmentation products in coincidence can reveal a surprisingly detailed picture of the dynamics. Determining the time evolution and quantum mechanical states involved leads to deeper understanding of molecular dynamics. Here in a combined experimental and theoretical study, we unambiguously separate the sequential breakup via D + + OD + intermediates, from other processes leading to the same D + + D + + O final products of double ionization of water by a single photon. Moreover, we experimentally identify, separate, and follow step by step, two pathways involving the b 1 Σ + and a 1 Δ electronic states of the intermediate OD + ion. Our classical trajectory calculations on the relevant potential energy surfaces reproduce well the measured data and, combined with the experiment, enable the determination of the internal energy and angular momentum distribution of the OD + intermediate.
Publisher: AIP Publishing
Date: 16-04-2012
DOI: 10.1063/1.3701762
Abstract: Photoelectron velocity map imaging is combined with one- and two-photon ionization to study the near threshold photoionization of the 2-butyne molecule. In this region, the photoabsorption and photoionization cross sections display a very intense broad feature that is assigned to an ℓ = 4, πg shape resonance. The effect of this shape resonance on the vibrational branching ratios and photoelectron angular distributions is explored. Theoretical calculations of the photoionization cross section and photoelectron angular distributions are in good agreement with the experiments. The results for 2-butyne are compared with those of acetylene, propyne, and 1-butyne, none of which show such significant enhancements near threshold, and the differences are rationalized in terms of the symmetries and orbital angular momenta of the highest occupied orbitals and the corresponding shape resonances. Expectations for larger alkynes and alkynyl radicals are also discussed. A preliminary measurement of the ionization energy of the 2-butyne dimer is also presented.
Publisher: American Physical Society (APS)
Date: 23-12-2020
Location: United States of America
Location: United States of America
Location: United States of America
No related grants have been discovered for Robert Lucchese.