Search for an excited state of the triton.
Negative pion from 600 MeV synchrocyclotron stopped in thin Li 6 target in search for excited states of triton
Coulson, L.↗
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Photoionization from excited states of helium
The cross sections for photoionization from the 2 1S, 2 3S, 2 1P and 2 3P excited states of helium are calculated for photoelectron energies below the n = 2 threshold of He(+) using Hylleraas bound state wave functions and 1s-2s-2p close coupling final state wave functions. The resonant structures associated with the lowest-lying 1S, 1P, 3P, and 1D autoionizing states of helium are found to be characterized by large values of the line profile parameter q. The cross sections and the photoelectron angular distribution asymmetry parameters for the P-states are calculated for various polarization states of the target atom and the incident photon. Experiments which would lead to the separate determinations of the S- and D- wave partial photoionization cross sections are discussed.
Jacobs, V. L.↗
Determination of excited state molecular structures from time-resolved gas-phase X-ray scattering
We present a comprehensive investigation of a recently introduced method to determine transient structures of molecules in excited electronic states with sub-ångstrom resolution from time-resolved gas-phase scattering signals. The method, which is examined using time-resolved X-ray scattering data measured on the molecule N-methylmorpholine (NMM) at the Linac Coherent Light Source (LCLS), compares the experimentally measured scattering patterns against the simulated patterns corresponding to a large pool of molecular structures to determine the full set of structural parameters. In addition, we examine the influence of vibrational state distributions and find the effect negligible within the current experimental detection limits, despite that the molecules have a comparatively high internal vibrational energy. Here, the excited state structures determined using three structure pools generated using three different computational methods are in good agreement, demonstrating that the procedure is largely independent of the computational chemistry method employed as long as the pool is sufficiently expansive in the vicinity of the sought structure and dense enough to yield good matches to the experimental patterns.
74 ATOMIC AND MOLECULAR PHYSICS↗
Exploring far-from-equilibrium ultrafast polarization control in ferroelectric oxides with excited-state neural network quantum molecular dynamics
Ferroelectric materials exhibit a rich range of complex polar topologies, but their study under far-from-equilibrium optical excitation has been largely unexplored because of the difficulty in modeling the multiple spatiotemporal scales involved quantum-mechanically. To study optical excitation at spatiotemporal scales where these topologies emerge, we have performed multiscale excited-state neural network quantum molecular dynamics simulations that integrate quantum-mechanical description of electronic excitation and billion-atom machine learning molecular dynamics to describe ultrafast polarization control in an archetypal ferroelectric oxide, lead titanate. Far-from-equilibrium quantum simulations reveal a marked photo-induced change in the electronic energy landscape and resulting cross-over from ferroelectric to octahedral tilting topological dynamics within picoseconds. The coupling and frustration of these dynamics, in turn, create topological defects in the form of polar strings. The demonstrated nexus of multiscale quantum simulation and machine learning will boost not only the emerging field of ferroelectric topotronics but also broader optoelectronic applications.
36 MATERIALS SCIENCE↗
Generalized single excitation configuration interaction: an investigation into the impact of the inclusion of non-orthogonality on the calculation of core-excited states
In this paper, we investigate different non-orthogonal generalizations of the configuration interaction with single substitutions (CIS) method for the calculation of core-excited states. Fully non-orthogonal CIS (NOCIS) has been described previously for species with singlet and doublet ground states, and this paper reports the extension to molecules in their triplet ground state. In addition to NOCIS, we present a novel method, one-center NOCIS (1C-NOCIS), for open-shell molecules which is intermediate between NOCIS and the computationally less demanding static exchange approximation (STEX). We explore this hierarchy of spin-pure methods for core excitations of molecules with singlet, doublet, and triplet ground states. We conclude that, while NOCIS provides the best results and preserves the spatial symmetry of the wavefunction, 1C-NOCIS retains much of the accuracy of NOCIS at a dramatically reduced cost. For molecules with closed-shell ground states, STEX and 1C-NOCIS are identical.
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
Spectroscopic evidence of spin-state excitation in d-electron correlated semiconductor FeSb 2
Iron antimonide (FeSb 2 ) has been investigated for decades due to its puzzling electronic properties. It undergoes the temperature-controlled transition from an insulator to an ill-defined metal, with a cross-over from diamagnetism to paramagnetism. Extensive efforts have been made to uncover the underlying mechanism, but a consensus has yet to be reached. While macroscopic transport and magnetic measurements can be explained by different theoretical proposals, the essential spectroscopic evidence required to distinguish the physical origin is missing. In this paper, through the use of X-ray absorption spectroscopy and atomic multiplet simulations, we have observed the mixed spin states of 3d 6 configuration in FeSb 2 . Furthermore, we reveal that the enhancement of the conductivity, whether induced by temperature or doping, is characterized by populating the high-spin state from the low-spin state. Our work constitutes vital spectroscopic evidence that the electrical/magnetical transition in FeSb 2 is directly associated with the spin-state excitation.
74 ATOMIC AND MOLECULAR PHYSICS↗
Nonadiabatic Dynamics Simulation of the Wavelength-Dependent Photochemistry of Azobenzene Excited to the nπ* and ππ* Excited States
Azobenzene is one of the most ubiquitous photoswitches in photochemistry and a prototypical model for photoisomerizing systems. Despite this, its wavelength-dependent photochemistry has puzzled researchers for decades. Upon excitation to the higher energy ππ* excited state instead of the dipole-forbidden nπ* state, the quantum yield of isomerization from trans- to cis-azobenzene is halved. The difficulties associated with unambiguously resolving this effect both experimentally and theoretically have contributed to lasting controversies regarding the photochemistry of azobenzene. Here, we systematically characterize the dynamic photoreaction pathways of azobenzene by performing first-principles simulations of the nonadiabatic dynamics following excitation to both the ππ* and the nπ* states. In this work, we demonstrate that ground-state recovery is mediated by two distinct S1 decay pathways: a reactive twisting pathway and an unreactive planar pathway. Increased preference for the unreactive pathway upon ππ* excitation largely accounts for the wavelength-dependent behavior observed in azobenzene.
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
Short-lived metal-centered excited state initiates iron-methionine photodissociation in ferrous cytochrome c
Abstract The dynamics of photodissociation and recombination in heme proteins represent an archetypical photochemical reaction widely used to understand the interplay between chemical dynamics and reaction environment. We report a study of the photodissociation mechanism for the Fe(II)-S bond between the heme iron and methionine sulfur of ferrous cytochrome c . This bond dissociation is an essential step in the conversion of cytochrome c from an electron transfer protein to a peroxidase enzyme. We use ultrafast X-ray solution scattering to follow the dynamics of Fe(II)-S bond dissociation and 1 s 3 p (Kβ) X-ray emission spectroscopy to follow the dynamics of the iron charge and spin multiplicity during bond dissociation. From these measurements, we conclude that the formation of a triplet metal-centered excited state with anti-bonding Fe(II)-S interactions triggers the bond dissociation and precedes the formation of the metastable Fe high-spin quintet state.
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
Dyads with tunable near-infrared donor–acceptor excited-state energy gaps: molecular design and Förster analysis for ultrafast energy transfer
Nine dyads composed of bacteriochlorins were prepared to investigate excited-state energy transfer (FRET) processes.
Jing, Haoyu↗
Semiclassical study of the quenching of excited-state fluorine atom by hydrogen molecule - Comparison between reactive and nonreactive processes
Semiclassical calculations are carried out for the quenching of excited-state fluorine atom by collinear collisions with hydrogen molecule. The overall quenching probability is the sum of two contributions: the reactive quenching probability associated with the formation of hydrogen fluoride and the nonreactive quenching probability leading to ground-state fluorine atom and hydrogen molecule. The reactive probability is greater in the threshold region of the collision energy, whereas the nonreactive probability dominates for energies above the threshold region.
Yuan, J.-M.↗
The high-ionization and excited-state interstellar lines in the Carina Nebula - A giant H II region in absorption
The dominant component of the highly ionized and excited-state interstellar species seen in the ultraviolet toward stars within the Carina Nebula has been found to have a heliocentric radial velocity of about -30 km/s. This velocity is known to correspond to the near edge of the expanding H II region, as shown by the double optical nebular emission lines and the single He I lambda 3889 nebular absorption line. It is also seen as a (nondominant) component in both the optical and ultraviolet low-ionization interstellar lines, discussed previously. Hence, the Carina Nebula provides a clear case in which the principal high-ionization interstellar features are associated with the hot stars against which they are observed; and a considerable range of absorption lines can provide physical information about the H II region. Also, the weaker zero-velocity, line-of-sight component in the high-ionization species can be measured in this direction relatively free from confusion by the material associated with the stars. There is, in addition, a pervasive high-ionization feature with a velocity of -90 km/s in this region, which has the relatively large value of N(C IV)/N(Si IV) = 4.5.
Walborn, N. R.↗
Development of Approaches to Model Excited State Charge and Energy Transfer in Solution
The development of next generation energy conversion and catalytic systems requires fundamental understanding of the interplay between photo-excitation and the resulting proton and electron transfer processes that occur in solution. To address these challenges requires accurate and efficient methods to compute ground and excited states, as well as the ability to treat the dynamics of energy transfer in the presence of solvent fluctuations. Our team is developing accurate and efficient theoretical models for solution phase reactions. These developments provide an improved understanding of photo-initiated excitations, electron transfer, and proton coupled electron transfer processes. Our research team brings together expertise in electron and nuclear dynamics (classical and quantum), electronic structure, and analysis of solvation networks. We are developing and validating techniques for modeling condensed phase charge and energy transfer and to simulate the methods to monitor them using optical and vibrational spectroscopy.
74 ATOMIC AND MOLECULAR PHYSICS↗
Jet-resolved vibronic structure in the higher excited states of N2O - Ultraviolet three-photon absorption spectroscopy from 80,000 to 90,000/cm
Ionization-detected UV multiphoton absorption spectroscopy of the excited states of N2O is presented, showing Rydberg structure within 20,000/cm of the first ionization threshold. Despite evidence for strong Rydberg-continuum coupling in the form of broadened bands and Fano line-shapes, the Rydberg structure persists, with atomic-like quantum defects and vibration structure well-matched with that of the ion. In the most clearly resolved spectrum, corresponding to the 3p(delta)1Pi state, Renner-Teller and Herzberg-Teller coupling of electronic and vibrational angular momentum are revealed. It is suggested that these mixings are properties of the N2O(+)Pi ion core.
Patsilinakou, E.↗
Theoretical characterization of the potential energy surface for H + N2 yields HN2. III - Calculations for the excited state surfaces
Additional calculations which characterize potential energy sources (PESs) for the excited 3A-double-prime state, for a bound 2(2A-prime) state, for HN2(+), and for the Rydberg states associated with HN2(+). It is anticipated that these excited state PESs will be important in interpreting and designing experiments to characterize the ground state HN2 species via neutralized ion beam techniques.
Walch, Stephen P.↗
Angular correlations in the ${e^+}{e^-}$ decay of excited states in $\mathrm{^8Be}$
Motivated by the recent observation of anomalous electron-positron angular correlations in the decay of the 18.15-MeV $\mathrm{1^+}$ excited states in $\mathrm{^8Be}$, we reexamine in detail the standard model expectations for these angular correlations. The 18.15-MeV state is above particle threshold, and several multipoles can contribute to its ${e^+}{e^-}$ decay. Here, we present the general theoretical expressions for ${e^+}{e^-}$ angular distributions for nuclear decay by $C0, C1, C2, M1, E1,$ and $E2$ multipoles, and we examine their relative contribution to the ${e^+}{e^-}$ decay of $\mathrm{^8Be}$ at 18.15 MeV. We find that this resonance is dominated by $M1$ to $E1$ decay, and that the ratio of $M1$ to $E1$ strength is a strong function of energy. This is in contrast to the original analysis of the ${e^+}{e^-}$ angular distributions, where the $M1/E1$ ratio was assumed to be a constant over the energy region ${E_p} = 0.8 – 1.2$ MeV. We find that the existence of a “bump” in the measured angular distribution is strongly dependent on the assumed $M1/E1$ ratio, with the present analysis finding the measured large-angle contributions to the ${e^+}{e^-}$ angular distribution to be lower than expectation. Thus, in the current analysis we find no evidence for axion decay in the 18.15-MeV resonance region of $\mathrm{^8Be}$.
6 ≤ A ≤ 19↗
Radiative electron-ion recombination into the first excited state of lithium
Li photoionization cross sections determined from spectral intensity measurements as function of threshold wavelength, discussing radiative electron-ion recombination into first excited state
Rothe, D. E.↗
Electron collision cross sections involving excited states
The vibrational excitation/deexcitation of vibrationally and rotationally hot N2 by electron impact, pertinent to the reactions in the flow field around a hypersonic space vehicle entering the planetary atmosphere, is calculatively investigated. It is found that the resonance position shifts to a lower energy when N2 is rotationally hot. Electron impact excitations between electronic excited states of N2 are studied using a multichannel treatment. The results show that the assumption that excited-excited cross sections are the same as ground-excited ones, and result in the same final state, is invalid. A more reliable set of data on N2 is provided.
Huo, Winifred M.↗
Excited-State Dynamics and Nonlinear Optical Properties of Hyperpolarizable Chromophores Based on Conjugated Bis(terpyridyl)Ru(II) and Palladium and Platinum Porphyrinic Components: Impact of Heavy Metals upon Supermolecular Electro-Optic Properties
A new series of strongly coupled oscillators based upon (porphinato)Pd, (porphinato)Pt, and bis(terpyridyl)-ruthenium(II) building blocks is described. These RuPPd, RuPPt, RuPPdRu, and RuPPtRu chromophores feature bis- (terpyridyl)Ru(II) moieties connected to the (porphinato)metal unit via an ethyne linker that bridges the 4!-terpyridyl and porphyrin macrocycle meso-carbon positions. Pump–probe transient optical data demonstrate sub-picosecond excited singlet-to-triplet-state relaxation. The relaxed lowest-energy triplet (T 1 ) excited states of these chromophores feature absorption manifolds that span the 800–1200 nm spectral region, microsecond triplet-state lifetimes, and large absorptive extinction coefficients [ε(T 1 → T n ) > 4 × 10 4 M –1 cm –1 ]. Dynamic hyperpolarizability (β λ ) values were determined from hyper-Rayleigh light scattering (HRS) measurements carried out at several incident irradiation wavelengths over the 800–1500 nm spectral region. Relative to benchmark RuPZn and RuPZnRu chromophores which showed large βHRS values over the 1200–1600 nm range, RuPPd, RuPPt, RuPPdRu, and RuPPtRu displayed large βHRS values over the 850–1200 nm region. Generalized Thomas–Kuhn sum (TKS) rules and experimental hyperpolarizability values were utilized to determine excited state-to-excited state transition dipole terms from experimental electronic absorption data and thus assessed frequency-dependent β λ values, including two- and three-level contributions for both β zzz and β xzx tensor components to the RuPPd, RuPPt, RuPPdRu, and RuPPtRu hyperpolarizability spectra. Furthermore, these analyses qualitatively rationalize how the βzzz and βxzx tensor elements influence the observed irradiation wavelength-dependent hyperpolarizability magnitudes. The TKS analysis suggests that supermolecules related to RuPPd, RuPPt, RuPPdRu, and RuPPtRu will likely feature intricate dependences of experimentally determined βHRS values as a function of irradiation wavelength that derive from substantial singlet–triplet mixing, and complex interactions among multiple different β tensor components that modulate the long wavelength regime of the nonlinear optical response.
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗