Nowdays, coupled cluster method belongs to one of the most used quantum chemical methods. However, the single-reference coupled cluster methods are not able to describe systems where the static correlation have an important role. Multireference coupled cluster methods developed in our group can describe both static and dy- namic correlation and can be used for problematic systems. Together with explicitly correlated wavefunction, which can properly describe the electronic cusp and speed up the convergence to the complete ba- sis set limit, they are able to calculate computationally demanding diradicals. Multireference CC calculations of tetramethylenethane have been perforemd and the performance of explicitly correlated version is discussed. Calculations of the isomerization of bicyclobu- tane using the multireference approach are presented as well. 1

Wave function based electronic structure methods have became a robust and reliable tool for the prediction and interpretation of the results of chemical experiments. However, they suffer from very steep scaling behavior with respect to an increase in the size of the system as well as very slow convergence of the correlation energy with respect to the basis set size. Thus these methods are limited to small systems of up to a dozen atoms. The first of these issues can be efficiently resolved by exploiting the local nature of electron correlation effects while the second problem is alleviated by the use of explicitly correlated R12/F12 methods. Since R12/F12 methods are central to this work, we start by reviewing their modern formulation. Next, we present the explicitly correlated second-order Mo ller-Plesset (MP2-F12) method in which all nontrivial post-mean-field steps are formulated with linear computational complexity in system size [Pavov{s}evi'c et al., {em J. Chem. Phys.} {bf 144}, 144109 (2016)]. The two key ideas are the use of pair-natural orbitals for compact representation of wave function amplitudes and the use of domain approximation to impose the block sparsity. This development utilizes the concepts for sparse representation of tensors described in the context of the DLPNO-MP2 method by Neese, Valeev and co-workers [Pinski et al., {em J. Chem. Phys.} {bf 143}, 034108 (2015)]. Novel developments reported here include the use of domains not only for the projected atomic orbitals, but also for the complementary auxiliary basis set (CABS) used to approximate the three- and four-electron integrals of the F12 theory, and a simplification of the standard B intermediate of the F12 theory that avoids computation of four-index two-electron integrals that involve two CABS indices. For quasi-1-dimensional systems (n-alkanes) the bigO{N} DLPNO-MP2-F12 method becomes less expensive than the conventional bigO{N^{5}} MP2-F12 for $n$ between 10 and 15, for double- and triple-zeta basis sets; for the largest alkane, C$_{200}$H$_{402}$, in def2-TZVP basis the observed computational complexity is $N^{sim1.6}$, largely due to the cubic cost of computing the mean-field operators. The method reproduces the canonical MP2-F12 energy with high precision: 99.9% of the canonical correlation energy is recovered with the default truncation parameters. Although its cost is significantly higher than that of DLPNO-MP2 method, the cost increase is compensated by the great reduction of the basis set error due to explicit correlation. We extend this formalism to develop a linear-scaling coupled-cluster singles and doubles with perturbative inclusion of triples and explicitly correlated geminals [Pavov{s}evi'c et al., {em J. Chem. Phys.} {bf 146}, 174108 (2017)]. Even for conservative truncation levels, the method rapidly reaches near-linear complexity in realistic basis sets; e.g., an effective scaling exponent of 1.49 was obtained for n-alkanes with up to 200 carbon atoms in a def2-TZVP basis set. The robustness of the method is benchmarked against the massively parallel implementation of the conventional explicitly correlated coupled-cluster for a 20-water cluster; the total dissociation energy of the cluster ($sim$186 kcal/mol) is affected by the reduced-scaling approximations by only $sim$0.4 kcal/mol. The reduced-scaling explicitly correlated CCSD(T) method is used to examine the binding energies of several systems in the L7 benchmark data set of noncovalent interactions. Additionally, we discuss a massively parallel implementation of the Laplace transform perturbative triple correction (T) to the DF-CCSD energy within density fitting framework. This work is closely related to the work by Scuseria and co-workers [Constans et al., {em J. Chem. Phys.} {bf 113}, 10451 (2000)]. The accuracy of quadrature with respect to the number of quadrature points has been investigated on systems of the 18-water cluster, uracil dimer and pentacene dimer. In the case of the 18-water cluster, the $mu text{E}_{text{h}}$ accuracy is achieved with only 3 quadrature points. For the uracil dimer and pentacene dimer, 6 or more quadrature points are required to achieve $mu text{E}_{text{h}}$ accuracy; however, binding energy of $<$1 kcal/mol is obtained with 4 quadrature points. We observe an excellent strong scaling behavior on distributed-memory commodity cluster for the 18-water cluster. Furthermore, the Laplace transform formulation of (T) performs faster than the canonical (T) in the case of studied systems. The efficiency of the method has been furthermore tested on a DNA base-pair, a system with more than one thousand basis functions. Lastly, we discuss an explicitly correlated formalism for the second-order single-particle Green's function method (GF2-F12) that does not assume the popular diagonal approximation, and describes the energy dependence of the explicitly correlated terms [Pavov{s}evi'c et al., {em J. Chem. Phys.} {bf 147}, 121101 (2017)]. For small and medium organic molecules the basis set errors of ionization potentials of GF2-F12 are radically improved relative to GF2: the performance of GF2-F12/aug-cc-pVDZ is better than that of GF2/aug-cc-pVQZ, at a significantly lower cost. / Ph. D.

Single-particle Green's function method is a direct way of calculating electron binding energy, which relies on expanding the Fock subspace in a finite single-particle basis. However, these methods suffer from slow asymptotic decay of basis set incompleteness error. An energy-dependent explicitly correlated (F12) formalism for Green's function is presented that achieves faster convergence to the basis set limit. The renormalized second-order Green's function method (NR2-F12) scales as iterative N^5 where N is the system size. These methods are tested on a set of small (O21) and medium-sized (OAM24) organic molecules. The basis set incompleteness error in ionization potential (IP) obtained from the NR2-F12 method and aug-cc-pVDZ basis for OAM24 is 0.033 eV compared to 0.067 eV for NR2 method and aug-cc-pVQZ basis. Hence, accurate electron binding energies can be calculated at a lower cost using NR2-F12 method. For aug-cc-pVDZ basis, the electron binding energies obtained from NR2-F12 are comparable to EOM-IP-CCSD method that uses a CCSD reference and scales as iterative N^6. / Master of Science / Solving the non-relativistic time-independent Schrödinger equation is a central problem in quantum chemistry with the primary goal of finding the exact electronic wave function. Like all many-body problems, the applications of highly accurate electronic structure methods are limited to small molecules since they are computationally expensive. With scalable algorithms and parallel implementation of computer programs, the chemistry of large molecular systems can be investigated. Electron binding energies give an insight into the orbital picture of a molecule, which is manifested in chemical structure and properties of a molecule. Green’s function provides an alternative to wave function based methods to calculate ionization potential and electron affinity directly rather than solving for the wave function itself. For accurate electron binding energies, the wave function needs to be represented by large number of basis functions, which make these methods computationally expensive. Explicitly correlated electronic structure methods are designed to produce accurate results at a smaller basis set. This work investigates the use of explicitly correlated Green’s function methods to calculate electron binding energies of small and medium sized organic molecules. These results are compared to coupled cluster methods, which are known to provide accurate benchmarks in quantum chemistry.

Le but principal de ce travail est d'examiner la capacité des méthodes clusters couplés explicitement corrélées (CCSD(T)-F12) pour la génération des surface de potentiel (SEPs) multidimensionnelles à courte, moyenne et longue portée intermoléculaires et leur utilisation dans la détermination des spectres des systèmes van der Waals (vdW) et des données de collision sur une large gamme d'énergie de collision. Ceci a été fait par une comparaison directe des surfaces de potentiel et des résultats générés à partir de l'utilisation des méthodes clusters couplés standards avec simple, double et un traitement perturbatif des excitations triples (CCSD(T)) et explicitement corrélée CCSD(T)-F12. En effet, nous démontrons que la méthode CCSD(T)-F12 en connexion avec la base aug-cc-pVTZ est la méthode de choix pour la génération de ces surfaces de potentiel avec une très grande réduction du coût computationnel (temps CPU et occupation disque). Ceci est illustré à travers l'étude des systèmes vdW HCl/DCl-He et CO2 -CO2 qui sont importants pour l'astrophysique et les atmosphères planétaires. Pour HCl/DCl-He, nous avons comparé les résultats issus des SEPs explicitement corrélées et celles calculées avec les méthodes cluster couplés standards. Ces SEPs ont été générées le long des coordonnées intermonomères. A travers ces comparaisons, nous avons montré que l'utilisation des méthodes CCSD(T)-F12/aug-cc-pVTZ explicitement corrélées permet de dépasser la précision de l'approche CCSD(T)/CBS (prise comme référence) avec un coût computationnel très réduit. La qualité de la surface de potentiel explicitement corrélée a été vérifiée par le calcul des sections efficaces et des taux de collision d'excitation rotationnelle de HCl/DCl par He. Par la suite, Nous étendons, notre étude aux systèmes moléculaires plus larges à travers l'étude du dimère de dioxyde de carbone,(CO2 )2 . Ainsi, nous avons généré une SEP d'interaction à 4 dimensions pour le dimère de dioxyde de carbone (CO2 )2 en utilisant la méthode CCSD(T)-F12/aug-cc-pVTZ qui a été comparée avec d'autres surfaces et spécialement avec celle générée par les approches de référence CCSD(T)/CBS et SAPT. Cette comparaison a bien prouvé la performance des méthodes explicitement corrélées pour la description de la corrélation électronique. Ceci, a été validé par des calculs de dynamique qui ont permis de déterminer le second coefficient du viriel, le premier moment spectral et les niveaux vibrationnels du dimère de CO2 et leur comparaison aux résultats expérimentaux et théoriques existants. Nous recommandons donc l'utilisation de la méthode CCSD(T)-F12/aug-cc-pVTZ pour l'étude des interactions moléculaires impliquant des systèmes polyatomique-polyatomique faiblement liés / The main goal of this work is to examine the capabilities of explicitly correlated coupled cluster (CCSD(T)-F12) methods for the mapping of multidimensional potential energy surfaces (PESs) at short, medium and long intermolecular ranges and therefore their use in the determination of accurate collisional data for a wide range of collision energies after dynamical computations. This is done through close comparisons of these PESs and corresponding data to those deduced using standard coupled cluster approaches with perturbative treatment of triple excitations (CCSD(T)). Therefore, we definitely establish that CCSD(T)-F12 in connection with the aug-cc-pVTZ basis set is the method of choice for the generation of such accurate PESs with strong reduction of computational cost (CPU and disk occupancy). As a benchmark, we treated the rotational excitation induced by collision of HCl/DCl-He and CO2 -CO2 van der Waals molecular systems, which are relevant for astrophysics and planetary atmospheres, respectively. For HCl-He and DCl-He, we closely compared the results deduced from PESs calculated with explicitly correlated and standard coupled cluster methods. These PESs were generated over the intermonomer degrees of freedom. Through these comparisons, we have shown that the use of explicitly correlated CCSD(T)-F12/aug-cc-pVTZ method overcomes the accuracy of the reference approach CCSD(T) associated with the complete basis set (CBS) with a very low computational cost (2 orders of magnitude less). The quality of the explicitly correlated potential surface was verified by cross sections and collision rate calculations. Then, we extended our findings to the CO2 -CO2 larger molecular systems. Hence, we generated four-dimentional (4D) PES of the carbon dioxide dimer (CO2 )2 using the CCSD(T)-F12 method and we compared it with other surfaces specially with that generated by the CCSD(T)/CBS and SAPT approaches. Again, we established the performance of explicitly correlated method to account fully for electron correlation. This was validated after dynamical calculations, where second virial coefficient, first spectral moment and vibrational energies of the CO2 dimer were computed and compared to previous experimental and theoretical data. In total, we recommend the use of CCSD(T)/aug-cc-pVTZ method for the investigation of weak interactions occurring between polyatomic-polyatomic systems for a wide range of applications