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Impact parameter versions of two state and Born approximations to calculate single excitation cross sections of H atoms ground state collisions
Simple orbital ideas are used to describe the lowest two states of the peroxyformyl radical, and ab initio Hartree-Fock calculations in these states are reported. It is found that both states may be formed exothermically by association of O2 and HCO in their ground states; however, the excited state may decompose readily to OH and CO2. The possible role of such processes in oxidation of aldelydes is discussed.
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.
The use of laser-induced fluorescence to measure OH in the troposphere is discussed. It is noted that quantitative laser detection of OH requires knowledge of collisional processes affecting the measurements and interference effects due to OH generated by laser photolytic processes. Collisions induce quenching of the excited A-state, as well as vibrational and rotational energy transfer in the excited and ground states. It is noted that the state-specific nature of these processes is important, especially the rotational level dependence of quenching and vibrational transfer in excited OH. Also important is the temperature dependence according to which quenching cross sections sharply increase with decreasing temperature. Laboratory experiments studying these collisional processes are described, and their implications for laser detection of tropospheric OH are examined.
Time-resolved X-ray (Tr-XAS) and optical transient absorption (OTA) spectroscopy in the pico-microsecond time scale coupled with Density Functional theory calculations are applied to study the light-induced spin crossover processes of a Fe-based macrocyclic complex in solution. Tr-XAS analysis after light illumination shows the formation of a seven-coordinated high spin quintet metastable state which relaxes to a six-coordinated high spin configuration before decaying to ground state. Kinetic analysis of the macrocyclic complex reveals an unprecedented long-lived decay lifetime of ~42.6 µs. Comparative studies with a non-macrocyclic counterpart illustrate a significantly shortened ~568-old decay lifetime of ~75 ns, and highlight the importance of the ligand arrangement in stabilizing the reactivity of the excited state. Lastly, OTA analysis shows the seven-coordinated high spin state to be formed within ~6.2 ps. Finally, these findings provide a complete understanding of the spin crossover reaction and relaxation pathways of the macrocyclic complex, and reveal the importance of a flexible coordination environment for their rational design.
Here, we report the observation of a small, yet remarkably stable, metal-free hexacyanodiborate dianion [B 2 (CN) 6 ] 2– in the gas phase. Negative ion photoelectron spectroscopy (NIPES) was employed to measure its spectra at multiple laser wavelengths, yielding a 1.9 eV electron binding energy (EBE) —a remarkably high value of electronic stability and a ~2.60 eV repulsive Coulomb barrier (RCB) for electron detachment. This rationalizes the observation of this dianion, although homolytic charge-separation dissociation into two [B(CN) 3 ] •– is energetically favorable. Quantum chemical calculations demonstrate a $D_{3d}$ staggered conformation for both the dianion and radical monoanion, and the calculated EBE and RCB match the experimental values well. The simulated density of states spectrum reproduces all measured electronic transitions, while the simulated vibrational progressions for the ground state transition cover a much narrower EBE range compared to the experimental band, indicating appreciable auto-photodetachment via electronically excited dianion resonances
We report on the fault-tolerant operation of logical qubits on a neutral atom quantum computer, with logical performance surpassing physical performance for multiple circuits including Bell state preparation (12x error reduction), random circuits (15x), and a prototype Anderson Impurity Model ground state solver for materials science applications (up to 6x, non-fault-tolerantly). The logical qubits are implemented via the [[4, 2, 2]] code (C 4 ). Our work constitutes the first complete realization of the benchmarking protocol proposed by Gottesman 2016 demonstrating results consistent with fault tolerance. In light of recent advances on applying concatenated C 4 /C 6 detection codes to achieve error correction with high code rates and thresholds, our work can be regarded as a building block towards a practical scheme for fault tolerant quantum computation. Our demonstration of a materials science application with logical qubits particularly demonstrates the immediate value of these techniques on current experiments.
We extend the DeePMD neural network architecture to predict electronic structure properties necessary to perform non-adiabatic dynamics simulations. While learning the excited state energies and forces follows a straightforward extension of the DeePMD approach for ground-state energies and forces, how to learn the map between the non-adiabatic coupling vectors (NACV) and the local chemical environment descriptors of DeePMD is less trivial. Most implementations of machine-learning-based non-adiabatic dynamics inherently approximate the NACVs, with an underlying assumption that the energy-difference-scaled NACVs are conservative fields. We overcome this approximation, implementing the method recently introduced by Richardson [J. Chem. Phys. 158, 011102 (2023)], which learns the symmetric dyad of the energy-difference-scaled NACV. Furthermore, the efficiency and accuracy of our neural network architecture are demonstrated through the example of the methaniminium cation CH 2 NH 2 + .
A detailed exploration of the f-atomic orbital occupancy space for UO2 is performed using a first principles approach based on density functional theory (DFT), employing a full hybrid functional within a systematic basis set. Specifically, the PBE0 functional is combined with an occupancy biasing scheme implemented in a wavelet-based algorithm which is adapted to large supercells. The results are compared with previous DFT + U calculations reported in the literature, while dynamical mean field theory is also performed to provide a further base for comparison. This work shows that the computational complexity of the energy landscape of a correlated f-electron oxide is much richer than has previously been demonstrated. The resulting calculations provide evidence of the existence of multiple previously unexplored metastable electronic states of UO 2 , including those with energies which are lower than previously reported ground states.
The neutron-deficient 188 Bi and 188 Po isotopes have been studied by γ-ray spectroscopy using the recoil-decay tagging technique with the Argonne Gas-Filled Analyzer. A new 0.25(5)-μs isomeric state and a prompt cascade formed by 319-, 366-, and 462-keV γ rays have been established on top of the (10¯) α -decaying isomer in 188 Bi. The first excited (2 + ) state in 188 Po was identified, its excitation energy of 242(2) keV continues the nearly constant trend for the first 2 + states in 190, 192,194 Po. Here, the state is most likely a member of a prolate rotational band built on the ground state, albeit mixing with other coexisting configurations cannot be excluded. The new results obtained in the present work provide new information to shape coexistence in bismuth and polonium isotopes near the neutron midshell at N = 104 . In this mass region, a reduction in the prompt γ-ray yield obtained with recoil decay tagging was observed for a few nuclides, and the possible reasons are presented.
In this article, we explore a feedback-control protocol in different quantum field theories (QFTs) to study the quantum correlation in nonunitary evolution of quantum systems. Traditional studies on QFTs focus on quantum entanglement of pure states under the unitary evolution, however, we examine quantum correlation in mixed states using quantum energy teleportation (QET), which is an energy transfer protocol by utilizing ground state entanglement, and introduce quantum discord as a measure. QET involves a midcircuit measurement, which disrupts pure state entanglement. Despite this, our analysis demonstrates that quantum discord maintains the correlation throughout the QET process. We conducted numerical analyses with benchmark models including the Nambu-Jona-Lasinio (NJL) model, revealing that quantum discord consistently acts as an order parameter for phase transitions. The model is extended in a way that it has both the chiral chemical potential and the chemical potential, which are useful to study the phase structures mimicking the chiral imbalance between left- and right- quarks coupled to the chirality density operator. In all cases we studied, the quantum discord behaved as an order parameter of the phase transition. Published by the American Physical Society 2024
We propose a general framework for studying two-dimensional (2D) topologically ordered states subject to local correlated errors and show that the resulting mixed state can display (imTO)—topological order that is not expected to occur in the ground state of 2D local gapped Hamiltonians. Specifically, we show that decoherence, previously interpreted as anyon condensation in a doubled Hilbert space, is more naturally phrased as, and provides a physical mechanism for, “gauging out” anyons in the original Hilbert space. We find that gauging out anyons generically results in imTO, with the decohered mixed state strongly symmetric under certain anomalous 1-form symmetries. This framework lays bare a striking connection between the decohered density matrix and , which can appear as anomalous surface states of three-dimensional topological orders. Through a series of examples, we show that the decohered state can display a classical memory, encode logical qubits (i.e., exhibit a quantum memory), and even host chiral or nonmodular topological order. We argue that a partial classification of imTO is given in terms of nonmodular braided-fusion categories. Published by the American Physical Society 2025
With the reactions of high flux neutrons, such as in a DT plasma, there is a prospect of seeing new kinds of neutron-nucleus reactions for the first time. If neutrons excite a heavy nucleus, for example, there is possibility of a second neutron reacting on excited states of the residual nucleus before that nucleus has de-excited to its ground state. The possibility of such reactions on excited states has rarely been considered. The cross section for neutron induced fission on the isomeric state of 235 U has been measured (D’Eer et al., Phys. Rev. C, 1988, 38: 1270–1276) and calculated (Younes et al., 2003, Maslov, 2007), and reactions on rotationally excited nuclear states has been calculated (Kawano et al., Phys. Rev. C, 2009, 80: 024611). In high flux plasmas, however, a much wider range of reactions is possible. We therefore need to consider excited states at much higher-energies than previously modeled, and then estimate whether second neutrons are likely to rescatter on those excited states. To determine the likelihood of such rescattering events, we first need to know the probable time series of nuclear decays of those excited states. The lifetimes of many low-lying states have been measured experimentally, but now we need to know the lifetimes of the many higher excited states that could be produced from incident 14 MeV neutrons. These are too numerous to be measured and also too numerous to be calculated individually, so statistical Hauser-Feshbach decay models are used. I show some lifetime calculations for 89 Y, 169 Tm, and 197 Au targets, and predictions for the number of rescattering events in plausible plasma scenarios.
Experimental differential scattering cross sections for excitation of helium by electron impact from its ground state to its 2(super 1)S state are presented at four incident electron energies in the range from 26 to 55.5 eV for scattering angles between 10 and 70 deg and at 81.6 eV for scattering angles between 10 and 80 deg. These cross sections are normalized and compared with results predicted by the Born approximation, the polarized Born approximation, and several other first-order approximations in which direct excitation is calculated in the Born approximation and exchange scattering in various Ochkur-like approximations.
Three strong asymmetric absorption features with short-wavelength wings extending 350 km/s from their respective line centers at 2061.6, 2068.2, and 2079.0 A appear in high-resolution UV spectral data (0.1 A) for the Be star Phi Per (B2 Ve4) obtained with the Balloon-borne Ultraviolet Stellar Spectrometer (BUSS) on the evening of September 16, 1976. These transitions are not resonance lines and have been identified as transitions of Fe III (UV 48) originating from a metastable state with an excitation of 5.01 eV. The relative populations of the metastable and ground states are independent of the dilution factor, allowing calculation of the mass-outflow rate for a generalized model. Thus, a mass-outflow rate of 5 hundred-billionths of a solar mass per year is obtained. These transitions are observable with IUE and represent an important tool for studying mass outflow in Be and shell stars.
Optical saturation is the phenomenon in which the laser-induced rates of absorption and spontaneous emission between two levels, induced by a laser, become comparable to or greater than the spontaneous emission and collision rates connecting these levels. This results in the excited state population N(u) acquiring a value of similar magnitude to that of the ground state, N(e). Under these conditions the observed fluorescence signal, which is proportional to N(u), is no longer linearly dependent on laser intensity I, but increases at a slower rate, and in principle ultimately becomes independent of I. A conceptual picture of optical saturation using a two-level picture is described. This is, however, inadequate for the description of a real experiment involving a molecule, such as OH, for several reasons, which will be explained briefly; these are the multi-level nature of the electronic states and energy transfer among them and effects due to spatial, spectral, and temporal fluctuations in the laser pulse.
Self consistent field molecular orbital method in LCAO /linear combination of atomic orbitals/ approximation applied to LiH ground state for potential energy curve
William Allan Bardeen (September 15, 1941 − November 18, 2025) was an American theoretical physicist who worked at the Fermi National Accelerator Laboratory. He is renowned for his foundational work on the chiral anomaly, the Adler-Bardeen theorem, the non-Abelian anomaly and gravitational anomalies. He was instrumental in the development of quantum chromodynamics and its applications, such as semileptonic decays and the Λ $\overline{MS}$ scheme frequently used in perturbative analysis of high energy processes involving strong interactions. Bardeen also played a major role in developing a theory of dynamical breaking of electroweak symmetry via top quark condensates, leading to one of the first composite Brout-Englert-Higgs boson models. His work on the chiral symmetry dynamics of heavy-light quark bound states correctly predicted abnormally long-lived resonances which are chiral symmetry partners of the ground state.