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Sudip Sasmal

Publications and source records attributed to Sudip Sasmal.

18 recordsLinked to original sources

Inverse optically-induced ring currents in ring-shaped molecules

Permanent electronic ring currents can be supported within a manifold of $Γ_E$ degenerate excited electronic states as $E_{\pm} = E_x \pm i E_y$ excitations. This requires at least a 3-fold-symmetry rotational axis or higher, and includes the subclass of ring-shaped molecules. In [Phys. Rev. Res. {\bf 3}, L042003 (2021)] we showed the existence of inverse-current manifolds, where the direction of the electronic ring-current in each degenerate state $E_\pm$ is opposite to the circular polarization of the generating light-fields. This phenomenon can be traced back to vibronic effects, namely the exchange of orbital angular momentum between the circulating electrons and vibrational modes with the required symmetry. Here we consider the case of fixed nuclei and find that ring-shaped molecular systems can posses inverse-current manifolds on a purely electronic-structure basis, i.e. without intervention of vibronic coupling. The effect is illustrated and explained first on a simple tight-binding model with cyclic symmetry, and then considering the {\it{ab initio}} electronic structure of benzene and sym-triazine. A framework for discriminating regular- and inverse-current $Γ_E$ manifolds in molecules using quantum chemistry calculations is provided.

physics.chem-ph

Compact sum-of-products form of the molecular electronic Hamiltonian based on canonical polyadic decomposition

We propose an approach to represent the second-quantized electronic Hamiltonian in a compact sum-of-products (SOP) form. The approach is based on the canonical polyadic decomposition (CPD) of the original Hamiltonian projected onto the sub-Fock spaces formed by groups of spin orbitals. The algorithm for obtaining the canonical polyadic form starts from an exact sum-of-products, which is then optimally compactified using an alternating least-squares procedure. We discuss the relation of this specific SOP with related forms, namely the Tucker format and the matrix product operator often used in conjunction with matrix product states. We benchmark the method on the electronic dynamics of an excited water molecule, trans-polyenes, and the charge migration in glycine upon inner-valence ionization. The quantum dynamics are performed with the multilayer multi-configuration time-dependent Hartree method in second quantization representation (MCTDH-SQR). Other methods based on tree-tensor Ansätze may profit from this general approach.

physics.chem-ph

Sum-of-products form of the molecular electronic Hamiltonian and application within the MCTDH method

We introduce two different approaches to represent the second-quantized electronic Hamiltonian in a sum-of-products form. These procedures aim at mitigating the quartic scaling of the number of terms in the Hamiltonian with respect to the number of spin orbitals, and thus enable applications to larger molecular systems. Here we describe the application of these approaches within the multi-configuration time-dependent Hartree framework. This approach is applied to the calculation of eigen energies of LiH and electronic ionization spectrum of H2O.

physics.chem-ph

A bosonic perspective on the classical mapping of fermionic quantum dynamics

We consider the application of the original Meyer-Miller (MM) Hamiltonian to mapping fermionic quantum dynamics to classical equations of motion. Non-interacting fermionic and bosonic systems share the same one-body density dynamics when evolving from the same initial many-body state. The MM classical mapping is exact for non-interacting bosons, and therefore it yields the exact time-dependent one-body density for non-interacting fermions as well. Starting from this observation, the MM mapping is compared to different mappings specific for fermionic systems, namely the spin mapping (SM) with and without including a Jordan-Wigner transformation, and the Li-Miller mapping (LMM). For non-interacting systems, the inclusion of fermionic anti-symmetry through the Jordan-Wigner transform does not lead to any improvement in the performance of the mappings and instead it worsens the classical description. For an interacting impurity model and for models of excitonic energy transfer, the MM and LMM mappings perform similarly, and in some cases the former outperforms the latter when compared to a full quantum description. The classical mappings are able to capture interference effects, both constructive and destructive, that originate from equivalent energy transfer pathways in the models.

physics.chem-ph

Exploration of interlacing and avoided crossings in a manifold of potential energy curves by a Unitary Group Adapted State Specific Multi-Reference Perturbation Theory (UGA-SSMRPT)

The Unitary Group Adapted State-Specific Multi-Reference Perturbation Theory (UGA-SSMRPT2) developed by Mukherjee et al [J. Comput. Chem. 2015, 36, 670] has successfully realized the goal of studying bond dissociation in a numerically stable, spin-preserving and size-consistent manner. In this paper, we explore and analyse the UGA-SSMRPT2 theory in the description of avoided crossings and interlacing between a manifold of states belonging to the same space-spin symmetry. In a state-specific formalism, since each state is an eigenstate of its own effective operator, to include the information of the other states requires the theory to be sufficiently accurate. Three different aspects of UGA-SSMRPT2 have been studied: (a) We introduce and develop the most rigorous version of UGA-SSMRPT2 which emerges from the rigorous version of UGA-SSMRCC utilizing a linearly independent virtual manifold; we call this the 'projection' version of UGA-SSMRPT2 denoted as UGA-SSMRPT2 Scheme P. We compare and contrast this approach with our earlier formulation that used extra sufficiency conditions via amplitude equations, which we will denote as UGA-SSMRPT2 Scheme A. (b) We present the results for a variety of electronic states of a set of molecules which display the striking accuracy of both the two versions of UGA-SSMRPT2; with respect to three different situations involving weakly avoided crossings, moderate/strongly avoided crossings and interlacing in a manifold of PECs of same symmetry. Accuracy of our results has been benchmarked against IC-MRCISD+Q. (c) For weakly avoided crossing between states displaying differently charged sectors in the asymptotes, the insufficient inclusion of state-specific orbital relaxation in a second order perturbative theory might lead to an artefact of double crossing between the pair of PECs.

physics.chem-ph

Non-adiabatic quantum dynamics without potential energy surfaces based on second-quantized electrons: application within the framework of the MCTDH method

A first principles quantum formalism to describe the non-adiabatic dynamics of electrons and nuclei based on a second quantization representation (SQR) of the electronic motion combined with the usual representation of the nuclear coordinates is introduced. This procedure circumvents the introduction of potential energy surfaces and non-adiabatic couplings, providing an alternative to the Born-Oppenheimer approximation. An important feature of the molecular Hamiltonian in the mixed first quantized representation for the nuclei and the SQR representation for the electrons is that all degrees of freedom, nuclear positions and electronic occupations, are distinguishable. This makes the approach compatible with various tensor decomposition \emph{ansätze} for the propagation of the nuclear-electronic wavefunction. Here, we describe the application of this formalism within the multi-configuration time-dependent Hartree (MCTDH) framework and its multilayer generalization, corresponding to Tucker and hierarchical Tucker tensor decompositions of the wavefunction, respectively. The approach is applied to the calculation of the photodissociation cross-section of the HeH$^+$ molecule under extreme ultraviolet irradiation, which features non-adiabatic effects and quantum interferences between the two possible fragmentation channels, He+H$^+$ and He$^+$+H. These calculations are compared with the usual description based on ab \emph{ab initio} potential energy surfaces and non-adiabatic coupling matrix elements, which fully agree. The proof-of-principle calculations serve to illustrate the advantages and drawbacks of this formalism, which are discussed in detail, as well as possible ways to overcome them.

physics.chem-ph

Relativistic double-ionization equation-of-motion coupled-cluster method: Application to low-lying doubly ionized states

The article deals with the extension of the relativistic double-ionization equation-of-motion coupled-cluster (DI-EOMCC) method [H. Pathak et al. Phys. Rev. A 90, 010501(R) (2014)] for the molecular systems. The Dirac-Coulomb (DC) Hamiltonian with four-component spinors is considered to take care of the relativistic effects. The implemented method is employed to compute a few low-lying doubly ionized states of noble gas atoms (Ar, Kr, Xe, and Rn) and Cl 2 , Br 2 , HBr, and HI. Additionally, we presented results with two intermediate schemes in the four-component relativistic DI-EOMCC framework to understand the role of electron correlation. The computed double ionization spectra for the atomic systems are compared with the values from the non-relativistic DI-EOMCC method with spin-orbit coupling (SOC) [Z. Wang et al. J. Chem. Phys. 142, 144109 (2015)] and the values from the National Institute of Science and Technology (NIST) database. Our atomic results are found to be in good agreement with the NIST values. Further, the obtained results for the molecular systems agree well with the available experimental values.

physics.chem-ph

Calculation of the magnetic hyperfine structure constant of alkali metals and alkaline earth metal ions using the relativistic coupled-cluster method

The Z-vector method in the relativistic coupled-cluster framework is used to calculate magnetic hyperfine structure constant ($A_J$) of alkali metals and singly charged alkaline earth metals in their ground state electronic configuration. The Z-vector results are in very good agreement with the experiment. The $A_J$ values of Li, Na, K, Rb, Cs, Be$^{+}$, Mg$^{+}$, Ca$^{+}$, and Sr$^{+}$ obtained in the Z-vector method are compared with the extended coupled-cluster results taken from Phys. Rev. A 91, 022512 (2015). The same basis and cutoff are used for the comparison purpose. The comparison shows that Z-vector method with the singles and double approximation can produce more precise wavefunction in the nuclear region than the ECC method.

physics.atom-ph

Calculation of hyperfine structure constants of small molecules using Z-vector method in the relativistic coupled-cluster framework

The Z-vector method in the relativistic coupled-cluster framework is employed to calculate the parallel and perpendicular components of the magnetic hyperfine structure constant of a few small alkaline earth hydrides (BeH, MgH, and CaH) and fluorides (MgF and CaF). We have compared our Z-vector results with the values calculated by the extended coupled-cluster (ECC) method reported in Phys. Rev. A 91 022512 (2015). All these results are compared with the available experimental values. The Z-vector results are found to be in better agreement with the experimental values than those of the ECC values.

physics.chem-ph

Electron-nucleus scalar-pseudoscalar interaction in PbF: Z-vector study in the relativistic coupled-cluster framework

The scalar-pseudoscalar interaction constant of PbF in its ground state electronic configuration is calculated using the Z-vector method in the relativistic coupled-cluster framework. The precise calculated value is very important to set upper bound limit on P,T-odd scalar-pseudoscalar interaction constant, k_s, from the experimentally observed P,T-odd frequency shift. Further, the ratio of the effective electric field to the scalar-pseudoscalar interaction constant is also calculated which is required to get an independent upper bound limit of electric dipole moment of electron, d_e, and k_s and how these (d_e and k_s) are interrelated is also presented here.

physics.atom-ph

Search for parity and time reversal violating effects in HgH: Relativistic coupled-cluster study

The high effective electric field ($E_\mathrm{eff}$) experienced by the unpaired electron in an atom or a molecule is one of the key ingredients in the success of electron electric dipole moment (eEDM) experiment and its precise calculation require a very accurate theory. We, therefore, employed the Z-vector method in the relativistic coupled-cluster framework and found that HgH has a very large $E_\mathrm{eff}$ value (123.2 GV/cm) which makes it a potential candidate for the next generation eEDM experiment. Our study also reveals that it has a large scalar-pseudoscalar ${\mathcal{P,T}}$-violating interaction constant, $W_\mathrm{s}$ = 284.2 kHz. To judge the accuracy of the obtained results we have calculated parallel and perpendicular magnetic HFS constants and compared with the available experimental values. The results of our calculation are found to be in nice agreement with the experimental values. Therefore, by looking at the HFS results we can say that both $E_\mathrm{eff}$ and $W_\mathrm{s}$ values are also very accurate. Further, We have derived the relationship between these quantities and the ratio which will help to get model independent value of eEDM and S-PS interaction constant.

physics.atom-ph

Relativistic equation-of-motion coupled-cluster method using open-shell reference wavefunction

The open-shell reference relativistic equation-of-motion coupled-cluster method within its four-component description is successfully implemented with the consideration of single- and double- excitation approximation. The one-body and two-body matrix elements required for the correlation calculation are generated using Dirac-Coulomb Hamiltonian. As a first attempt, the implemented method is employed to calculate a few of the low-lying ionized states of heavy atomic (Ag, Cs, Au, Fr, Lr) and valence ionization potential of molecular (HgH, PbF) systems, where the effect of relativity does really matter to obtain highly accurate results. Not only the relativistic effect, but also the effect of electron correlation is crucial in these heavy atomic and molecular systems. To justify the fact, we have taken two further approximations in the four-component relativistic equation-of-motion framework to quantify how the effect of electron correlation plays a role in the calculated values at different level of the approximation. All these calculated results are compared with the available experimental data as well as with other theoretically calculated values to judge the extent of accuracy obtained in our calculations. A nice agreement is achieved for all the considered systems which validates the performance of the open-shell reference relativistic equation-of-motion coupled-cluster method.

physics.atom-ph

Relativistic coupled-cluster study of RaF as a candidate for parity and time reversal violating interaction

We have employed both Z-vector method and the expectation value approach in the relativistic coupled-cluster framework to calculate the scalar-pseudoscalar (S-PS) P, T -odd interaction constant (W_s) and the effective electric field (Eeff) experienced by the unpaired electron in the ground electronic state of RaF. Further, the magnetic hyperfine structure constants of ^{223}Ra in RaF and ^{223}Ra+ are also calculated and compared with the experimental values wherever available to judge the extent of accuracy obtained in the employed methods. The outcome of our study reveals that the Z-vector method is superior than the expectation value approach in terms of accuracy obtained for the calculation of ground state property. The Z-vector calculation shows that RaF has a high E_eff (52.5 GV/cm) and W_s (141.2 kHz) which makes it a potential candidate for the eEDM experiment.

physics.atom-ph

Relativistic equation-of-motion coupled-cluster method for the electron attachment problem

The article considers the successful implementation of relativistic equation-of-motion coupled cluster method for the electron attachment problem (EA-EOMCC) at the level of single- and double- excitation approximation. The implemented relativistic EA-EOMCC method is employed to calculate ionization potential values of alkali metal atoms (Li, Na, K, Rb, Cs, Fr) and the vertical electron affinity values of LiX (X = H, F, Cl, Br), NaY (Y = H, F, Cl) starting from their closed-shell configuration. Both four-component and exact two-component calculations are done for all the opted systems. Further, we have shown the effect of spin-orbit interaction considering the atomic systems. The results of our atomic calculations are compared with the values from the NIST database and the results are found to be very accurate (< 1 %).

physics.atom-ph

Calculation of P,T-odd interaction constant of PbF using Z-vector method in the relativistic coupled-cluster framework

The effective electric field experienced by the unpaired electron in the ground state of PbF, which is a potential candidate in the search of electron electric dipole moment due to some special characteristics, is calculated using Z-vector method in the coupled cluster single- and double- excitation approximation with four component Dirac spinor. This is an important quantity to set the upper bound limit of the electron electric dipole moment. Further, we have calculated molecular dipole moment and parallel magnetic hyperfine structure constant (A$_\|$) of $^{207}$Pb in PbF to test the accuracy of the wave function obtained in the Z-vector method. The outcome of our calculations clearly suggests that the core electrons have significant contribution to the "atom in compound (AIC)" properties.

physics.atom-ph

Relativistic extended coupled cluster method for magnetic hyperfine structure constant

This article deals with the general implementation of 4-component spinor relativistic extended coupled cluster (ECC) method to calculate first order property of atoms and molecules in their open-shell ground state configuration. The implemented relativistic ECC is employed to calculate hyperfine structure (HFS) constant of alkali metals (Li, Na, K, Rb and Cs), singly charged alkaline earth metal atoms (Be+, Mg+, Ca+ and Sr+) and molecules (BeH, MgF and CaH). We have compared our ECC results with the calculations based on restricted active space configuration interaction (RAS-CI) method. Our results are in better agreement with the available experimental values than those of the RAS-CI values.

physics.chem-ph

Implementation of Z-vector method in the relativistic coupled cluster framework to calculate first order energy derivatives: Application to SrF molecule

The molecular dipole moment and magnetic hyperfine structure constant demand an accurate wavefunction far from the nucleus and in near nuclear region, respectively. We, therefore, employ the so-called Z-vector method in the domain of relativistic coupled cluster theory to calculate the first order property of molecular systems in their open-shell ground state configuration. The implemented method is applied to calculate molecular dipole moment and parallel component of the magnetic hyperfine structure constant of SrF molecule. The results of our calculation are compared with the experimental and other available theoretically calculated values. We are successful in achieving good accordance with the experimental results. The result of our calculation of molecular dipole moment is in the accuracy of ~? 0.5 %, which is clearly an improvement over the previous calculation based on the expectation value method in the four component coupled cluster framework [V. S. Prasannaa et al, Phys. Rev. A 90, 052507 (2014)] and it is the best calculated value till date. Thus, it can be inferred that the Z vector method can provide an accurate wavefunction in both near and far nuclear region, which is evident from our calculated results.

physics.chem-ph

Relativistic equation-of-motion coupled-cluster method for the ionization problem: Application to molecules

We report the implementation of 4-component spinor relativistic equation-of-motion coupledcluster method within the single- and double- excitation approximation to calculate ionization potential (EOM-CCSD) of molecules. We have applied this method to calculate vertical ionization potentials of the molecules, XH(X=F, Cl, Br, I) along with Cl2 and Br2 in their closed-shell configuration. We have also presented intermediate results using 2-nd order many-body perturbation theory level in the EOM framework (EOM-MBPT(2)) to understand the role of electron correlation. All the calculated values are compared with the available experimental results. Our results are found to be in well agreement with the sophisticated experiments and relative deviation of less than 1% achieved for all the considered systems.

physics.chem-ph