Multireference Configuration Interaction Level Research Articles

Molecular structure and spectra of ytterbium dihalides from first principles

The molecular structure, vibrational frequencies, infrared intensities and electric dipole moments of ytterbium dihalides YbX2 (X = F, Cl, Br, I) in their ground electronic state are studied at the coupled-cluster singles, doubles and perturbative triples CCSD(T) level using a series of large all-electron basis sets together with the complete basis set (CBS) extrapolation procedure, and with both scalar-relativistic and spin–orbit coupling effects taken into account. Excitation energies of low-lying electronic states are calculated at the multireference configuration interaction, equation-of-motion CCSD and single-reference CCSD(T) levels of theory. For all of the molecules under study, the CCSD(T)/CBS equilibrium geometries are found to be non-linear (C2v symmetry). There is a rapid decrease in heights of the barriers to linearity on passing through the YbX2 molecular series from fluoride to iodide: 1587 → 261 → 110 → 7 (all in cm−1) for YbF2 → YbCl2 → YbBr2 → YbI2, respectively. The uncertainties in the molecular structure data published to date are discussed and resolved in the light of the present results.

Computational determination of the S1(Ã1A″) absorption spectra of HONO and DONO using full-dimensional neural network potential energy surfaces.

The Ã1A″ ← X̃1A' absorption spectra of HONO and DONO were simulated by a full six-dimensional quantum mechanical method based on the newly constructed potential energy surfaces for the ground and excited electronic states, which were represented by the neural network method utilizing over 36 000 abinitio energy points calculated at the multireference configuration interaction level with Davidson correction. The absorption spectrum of HONO/DONO comprises a superposition of the spectra from two isomers, namely, trans- and cis-HONO/DONO, due to their coexistence in the ground X̃1A' state. Our calculated spectra of both HONO and DONO were found to be in fairly good agreement with the experiment, including the energy positions and widths of the peaks. The dominant progression was assigned to the N=O stretch mode (20n) associated with trans-HONO/DONO, which can be attributed to the promotion of an electron to the π* orbital of N=O. Specifically, the resonances with higher vibrational quanta were found to be in the domain of the Feshbach-type resonances. The assignments of the spectra and mode specificity therein are discussed.

Coupled 3D (J ≥ 0) Time-Dependent Wave Packet Calculation for the F + H2 Reaction on Accurate Ab Initio Multi-State Diabatic Potential Energy Surfaces.

We had calculated adiabatic potential energy surfaces (PESs), nonadiabatic, and spin-orbit (SO) coupling terms among the lowest three electronic states (12A', 22A', and 12A″) of the F + H2 system using the multireference configuration interaction (MRCI) level of theory, and the adiabatic-to-diabatic transformation equations were solved to formulate the diabatic Hamiltonian matrix [J. Chem. Phys. 2020, 153, 174301] for the entire region of the nuclear configuration space. The accuracy of such diabatic PESs is explored by performing scattering calculations to evaluate integral cross sections (ICSs) and rate constants. The nonadiabatic and SO effects are studied by utilizing coupled 3D time-dependent wave packet formalism with zero and nonzero total angular momentum on multiple adiabatic/diabatic surfaces calculation. We depict the convergence profiles of reaction probabilities for the reactive as well as nonreactive processes on various electronic states at different collision energies with respect to total angular momentum including all helicity quantum numbers. Finally, total ICSs are calculated as functions of collision energies for the initial rovibrational state (v = 0, j = 0) of the H2 molecule along with the temperature-dependent rate coefficient, where those quantities are compared with previous theoretical and experimental results.

Potential energy surface and quantum dynamics calculation of SH2− (2A′) based on ab initio scaled external correlation correction

An accurate interatomic potential energy surface for ground state of SH2− is reported at the multireference configuration interaction level of theory using aug–cc–pVQZ basis set. The calculated ab initio energy points are utilized, after semi-empirically correcting the dynamical correlation by the many-body expansion-scaled external correlation method. To verify the accuracy of the potential energy surface, molecular reaction dynamics, including the relationship between reaction probability and collision energy, thermal rate constant, and integral scattering cross section are calculated by using the quantum time-dependent wave packet method. The final results show that our potential energy surface is accurate and the molecular reaction dynamics results are satisfactory, and the accurate potential energy surface and its dynamics results can also lay a foundation for the future experimental research of SH−-containing molecules.

He+ +N2 Charge Transfer Reaction: An Ab initio Analysis.

An ab initio analysis on the involved potential energy surfaces is presented for the investigation of the charge transfer mechanism for the He+ +N2 system. At high collision energy, as many as seven low-lying electronic states are observed to be involved in the charge transfer mechanism. Potential energy surfaces for these low-lying electronic states have been computed in the Jacobi scattering coordinates, applying multireference configuration interaction level of theory and aug-cc-pVQZ basis sets. Asymptotes for the ground and various excited states are assigned to mark the entrance (He+ +N2 ) and charge transfer channels (He+N2 + ). Nonadiabatic coupling matrix elements and quasi-diabatic potential energy surfaces have been computed for all seven states to rationalize the available experimental data on the charge transfer processes and to facilitate dynamics studies.

Accurate Full-Dimensional Global Diabatic Potential Energy Matrix for the Two Lowest-Lying Electronic States of the H + O2 ↔ HO + O Reaction.

A new and more accurate diabatic potential energy matrix (DPEM) is developed for the two lowest-lying electronic states of HO2, covering both the strong interaction region and reaction asymptotes. The ab initio calculations were performed at the Davidson corrected multireference configuration interaction level with the augmented correlation-consistent polarized valence quintuple-zeta basis set (MRCI+Q/AV5Z). The accuracy of the electronic structure calculations is validated by excellent agreement with the experimental HO2 equilibrium geometry, fundamental vibrational frequencies, and H + O2 ↔ OH + O reaction energy. Through the combination of an electronic angular momentum-method and a configuration interaction vector-based method, the mixing angle between the first two 2A″ states of HO2 was successfully determined. Elements of the 2×2 DPEM were fit to neural networks with a proper account of the complete nuclear permutation inversion symmetry of HO2. The DPEM correctly predicted the properties of conical intersection seams at linear and T-shape geometries, thus providing a reliable platform for studying both the spectroscopy of HO2 and the nonadiabatic dynamics for the H + O2 ↔ OH + O reaction.

Reaction dynamics of C(3P) + Si2(X $^{3}\Sigma ^-_g$ ) → Si(3P) + SiC(X 3Π) on a global CHIPR potential energy surface of the ground state Si2C(X 1A1)

ABSTRACT The dynamics of C(3P) + Si2(X $^{3}\Sigma ^-_g$ ) → Si(3P) + SiC(X 3Π) on its ground state Si2C(X 1A1) are of great significance in carbon-rich interstellar chemistry. Using the combined-hyperbolic-inverse-power-representation method, we construct the first global potential energy surface (PES) for the electronic ground state Si2C(X 1A1) based on a total of 4080 ab initio energy points, which are obtained at the Davidson-corrected internally contracted multireference configuration interaction level of theory. The topographical features of the newly constructed PES are examined in detail and show good agreement with previous theoretical and experimental studies. Finally, we investigate the C(3P) + Si2(X $^{3}\Sigma ^-_g$ ) → Si(3P) + SiC(X 3Π) reaction using the quasi-classical trajectory and time-dependent wave packet calculations, yielding reasonable integral cross sections and rate constants, which are expected to be useful for astrochemical modelling in carbon-rich interstellar environments.

Full-dimensional potential energy surface for the photodissociation of HNCO via its S1 band.

A full-dimensional potential energy surface (PES) for the first excited state S1(1A'') of HNCO has been built up by the neural network method based on more than 36 000 ab initio points, which were calculated at the multireference configuration interaction level with Davidson correction using the augmented correlation consistent polarized valence triple zeta basis set. It was found that two minima, namely, trans and cis isomers of HNCO, and another seven stationary points exist on the S1 PES for the two dissociation pathways: HNCO(S1) → H + NCO/NH + CO. Particularly, a new out-of-plane transition state between the two minima was found in this work, thanks to including all the degree of freedoms for this system. The adiabatic excitation energy of the S1(1A'') ← S0(1A') transition and dissociation energies D0(HNCO → H + NCO) and D0((HNCO →NH(a1Δ) + CO) calculated on the PES are in good agreement with experimental results. In addition, based on the newly constructed S1 PES, the percentage of products H + NCO in the photodissociation of HNCO(S1) was obtained by a quasi-classical trajectory method at the photon wavelengths ranging from 190 to 225 nm, which is in reasonably good agreement with earlier theoretical and experimental results. For the dissociation lifetimes of the trajectories, they were calculated to be less than 5 ps, which is also consistent with experimental observations.

Nonadiabatic quantum dynamics of the charge transfer reaction H+ + NO(X2Π) → H + NO+(X1Σ+).

Nonadiabatic quantum dynamics of the charge transfer (CT) reaction H+ + NO(X2Π) → H + NO+(X1Σ+) is investigated on a new diabatic potential energy matrix (PEM) including the 12A' and 22A' states of HNO+/HON+ at the multireference configuration interaction level with Davidson correction using a large basis set. The diabatization of the two coupled states was achieved by the adiabatic-to-diabatic transformation with a mixing angle and the final diabatic PEM was obtained by fitting each matrix element separately using a three-dimensional cubic spline interpolation including more than 22 000 ab initio points. The reaction was found to be dominated by the resonances supported by the double well associated with HNO+ and HON+ species, manifested by the oscillatory structures in the reaction probabilities and product rotational distributions. The product vibrational states were highly excited due to the large exothermicity of the reaction. Consistent with the complex-forming mechanism, the differential cross sections (DCSs) were found to be dominated by the forward and backward scatterings. A clear forward bias in the vibrational state resolved DCSs suggests that the non-statistical behavior of the reaction mainly comes from the low vibrational states of the product. In addition, the rate constants of the reaction in the temperature range from 50 to 500 K were computed for the first time and found to be in fairly good agreement with the available experimental results at 300 K. In particular, compared to other reactions involving neutral species in this system including N, O, and H atoms, such a CT reaction was found to be much more reactive, which has rate constants more than thirty times larger.

Potential energy surfaces for singlet and triplet states of the LiH2+ system and quasi-classical trajectory cross sections for H + LiH+ and H+ + LiH.

A new set of six accurate ab initio potential energy surfaces (PESs) is presented for the first three singlet and triplet states of LiH2+ (1,21A', 11A'', 1,23A', and 13A'' states, where four of them are investigated for the first time), which have allowed new detailed studies gaining a global view on this interesting system. These states are relevant for the study of the most important reactions of lithium chemistry in the early universe. More than 45 000 energy points were calculated using the multi-reference configuration interaction level of theory using explicitly correlated methods (ic-MRCI-F12), and the results obtained for each individual electronic state were fitted to an analytical function. Using quasiclassical trajectories and considering the initial diatomic fragment in the ground rovibrational state, we have determined the integral cross sections for the H + LiH+(X2Σ+, C2Π) and H+ + LiH(X1Σ+, B1Π) reactions. In these calculations all available reaction channels were considered: the chemically most important H or H+ transfer/abstraction as well as atom exchange and collision induced dissociation for up to 1.0 eV of collision energy.

New accurate diabatic potential energy surfaces for the two lowest 1A'' states of H2S and photodissociation dynamics in its first absorption band.

In this work, state-to-state photodissociation dynamics of H2S in its first absorption band has been studied quantum mechanically with a new set of coupled potential energy surfaces (PESs) for the first two 1A'' excited states, which were developed at the explicitly correlated internally contracted multi-reference configuration interaction level with the cc-pVQZ-F12 basis set and a large active space. The calculated absorption spectrum, product state distributions, and angular distributions are in excellent agreement with available experimental data, validating the accuracy of the PESs and the non-adiabatic couplings. Detailed analysis of the dynamics reveals that there are strong non-adiabatic couplings between the bound 11B1 and dissociative 11A2 states around the Franck-Condon region, leading to very fast predissociation to ro-vibrationally cold SH(X̃) fragments, during which marginal angular anisotropy of the PESs is involved. This study provides quantitatively accurate characterization of the electronic structure and detailed fragmentation dynamics of this prototypical photodissociation system, which is desirable for improving astrochemical modelling.

The feasibility of laser cooling: an investigation of ab initio of 88Sr35Cl including the hyperfine structure

ABSTRACT A promising laser cooling candidate molecule is essential for laser cooling experiments. In this study, the possibility of laser cooling an 88Sr35Cl molecule is investigated using an ab initio method. Seven low-lying Λ-S and six Ω electronic states of the 88Sr35Cl molecule are calculated at a multi-reference configuration interaction level of theory. Spectral constants of bound states of fitted values are in good agreement with experimental values, which are better than the previously obtained theoretical data for higher excitation states. The resulting permanent and transition dipole moments near the equilibrium bond length are close to the theoretical values. Potential energy curves and transition dipole moments are used for obtaining highly diagonally distributed Franck-Condon factors for the A2Π → X2Σ+ transition using the LEVEL program. A short radiative lifetime of the A2Π state is determined; a laser cooling scheme is designed in the vibration level that requires a cooling main laser beam and two repumping laser beams. Transition spectral data of hyperfine energy levels with errors relative to the experimental data do not exceed −0.25∼0.19 MHz when using a quantum effective Hamiltonian approach. This study provides a helpful reference for experimental observation and operation of laser cooling the 88Sr35Cl molecule.

The many-body expansion for metals. I. The alkaline earth metals Be, Mg, and Ca

We examine the many-body expansion (MBE) for alkaline earth metal clusters, Ben, Mgn, Can (n = 4, 5, 6), at the Møller–Plesset second order perturbation theory, coupled-cluster singles and doubles with perturbative triples, multi-reference perturbation theory, and multi-reference configuration interaction levels of theory. The magnitude of each term in the MBE is evaluated for several geometrical configurations. We find that the behavior of the MBE for these clusters depends strongly on the geometrical arrangement and, to a lesser extent, on the level of theory used. Another factor that affects the MBE is the in situ (ground or excited) electronic state of the individual atoms in the cluster. For most geometries, the three-body term is the largest, followed by a steady decrease in absolute energy for subsequent terms. Though these systems exhibit non-negligible multi-reference effects, there was little qualitative difference in the MBE when employing single vs multi-reference methods. Useful insights into the connectivity and stability of these clusters have been drawn from the respective potential energy surfaces and quasi-atomic orbitals for the various dimers, trimers, and tetramers. Through these analyses, we investigate the similarities and differences in the binding energies of different-sized clusters for these metals.

ExoMol line lists – XLVI. Empirical rovibronic spectra of silicon mononitrate (SiN) covering the six lowest electronic states and four isotopologues

ABSTRACT Silicon mononitride (28Si14N, 29Si14N, 30Si14N, 28Si15N) line lists covering infrared, visible, and ultraviolet regions are presented. The SiNful line lists produced by ExoMol include rovibronic transitions between six electronic states: $X\, {}^{2}\Sigma ^{+}$, $A\, {}^{2}\Pi$, $B\, {}^{2}\Sigma ^{+}$, $D\, {}^{2}\Delta$, $a\, {}^{4}\Sigma ^{+}$, $b\, {}^{4}\Pi$. The ab initio potential energy and coupling curves, computed at the multireference configuration interaction (MRCI/aug-cc-pVQZ) level of theory, are refined for the observed states by fitting their analytical representations to 1052 experimentally derived SiN energy levels determined from rovibronic bands belonging to the X–X, A–X, and B–X electronic systems through the MARVEL procedure. The SiNful line lists are compared to previously observed spectra, recorded and calculated lifetimes, and previously calculated partition functions. SiNful is available via the www.exomol.com database.

Fano-Feshbach formalism applied to the calculation of autoionization widths through analytic continuation.

A method to calculate the autoionization width from a discretized pseudo-spectrum is proposed. This method relies on an analytic continuation of Green's function within the Fano-Feshbach formalism. The pseudo-spectrum is obtained at the multireference configuration interaction level in a square-integrable basis set, commonly found in quantum chemistry software. Few states around the desired resonance are needed to perform the analytic continuation. This method was applied to atomic (He and Ne) and molecular (HF and benzene) systems, and the results for the autoionization width show good agreement with the available theoretical and experimental values.

Experimental and theoretical investigation of excited g-symmetry states of Cu2

A new set of rovibronic terms in the range between ∼37000 and 39000cm-1 is reported for the copper dimer isotopologues 63Cu2 and 63Cu65Cu. These terms were measured by two-color four-wave mixing spectroscopy yielding rotationally resolved vibronic bands at a resolution ∼0.04cm-1. The complex spectral structure is analyzed and a tentative assignment of a new electronic state of gerade symmetry named {36.9}0g+ is proposed. The assignment is corroborated by ab initio calculations carried out at the multi-reference configuration interaction level of theory.

A neural network potential energy surface and quantum dynamics studies for the Ca+(2S) + H2 → CaH+ + H reaction.

Reactive collisions of Ca+ ions with H2 molecules play a crucial role in ultracold chemistry, quantum information and other cutting-edge fields, and have been widely studied experimentally, but the corresponding theoretical studies have not been reported due to the lack of an applicable potential energy surface (PES). Herein, a globally accurate PES of the ground-state CaH2+ is constructed using the permutation invariant polynomial neural network method based on 27 780 ab initio points calculated at the multi-reference configuration interaction level. On the new PES, the quantum time-dependent wave packet calculations are performed to study the dynamics mechanisms of the Ca+(2S) + H2(ν0 = 0, j0 = 0) → CaH+ + H reaction. The calculated results suggest that the reaction follows a direct abstraction process when the collision energy is below 5.0 eV. The dynamics results would have a great reference significance for the experimental research of this reactive system at a finer level, and further dynamics studies, such as the effects of isotope substitution and rovibrational excitations of the reactant molecule, could be carried out on this newly constructed PES.

An accurate many-body expansion potential energy surface for SiH2 (11 A') using a switching function formalism.

An accurate many-body expansion potential energy surface for the ground state of SiH2 is reported. To warrant the correct behavior at the Si (1D) + H2 (X1Σ+g) dissociation channels involving silicon in the first excited Si (1D) and ground Si (3P) states, a switching function formalism has been utilized. A great deal of ab initio points based on aug-cc-pV(Q+d)Z and aug-cc-pV(5+d)Z basis sets are utilized at the multi-reference configuration interaction level using the full-valence-complete-active-space wave function as the reference. Subsequently the calculated energies are corrected via a many-body expansion method to extrapolate to the complete basis set limit. The topographic features of the novel many-body expansion global potential energy surface are studied in detail, showing a good agreement with the theoretical and experimental results in the literature. Moreover, the integral cross-section of the Si (1D) + H2 (X1Σ+g) → H (2S) + SiH (X2Π) reaction has been calculated using the time-dependent wave packet method, which provides support for the reliability of the title potential energy surface. This work can serve as the foundation for the study of Si (1D) + H2 (X1Σ+g) reaction kinetics, and for the construction of the larger multibody expansion potential energy surface of silicon/hydrogen containing systems.

An accurate many-body expansion potential energy surface for AlH2 (22A') and quantum dynamics in Al(3P) + H2 (v0 = 0-3, j0 = 0, 2, 4, 6) collisions.

An accurate potential energy surface is constructed for the excited state of AlH2 by fitting extensive ab initio points calculated at the multi-reference configuration interaction level based on aug-cc-pV(Q+d)Z and aug-cc-pV(5+d)Z basis sets. All the calculated energies are corrected via the many-body expansion method and extrapolated to the complete basis set limit. The various topographic features of the new potential energy surface are investigated to demonstrate the correct behavior of Al(3P) + H2(X1Σg+) and AlH(a3Π) + H(2S) dissociation limits. By employing the time-dependent wave packet approach, the integral scattering cross-sections obtained from the Coriolis coupling calculation and the centrifugal sudden approximation, respectively, are compared in detail and show that the former has a higher effect on the reaction. Moreover, the thermal rate constants for Al(3P) + H2 (v0 = 0-3, j0 = 0, 2, 4, 6) in the temperature range of 0-5000 K are calculated, thereby providing insights into the influence of ro-vibrational quantum numbers on the thermal rate constants.

Globally Accurate Potential Energy Surface for BH2+2(13A') Using the Switching Function Formalism.

A great number of ab initio energy points are calculated using the aug-cc-pV(Q,5)Z basis sets at the multireference configuration interaction level and extrapolated to the complete basis set limit. An exact three-dimensional potential energy surface of the ground-state BH2+ is obtained. A switching function is developed to model the transition of B+(3P) to B+(1S) to guarantee the reliable behavior at B+(3P) + H2(X1∑g+) and BH+(X2∑+) + H(2S) dissociation limits. The various topographic features of the new global potential energy surface are discussed in detail, showing a good agreement with the previous results from the theory. The quasi-classical trajectory method is utilized to calculate the integral cross sections of the B+(3P) + H2(X1∑g+) (v = 0, j = 0) → BH+(X2∑+) + H(2S) reaction, which can provide another support for reliability of the title potential energy surface.