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  1. Article ; Online: A correctly scaling rigorously spin-adapted and spin-complete open-shell CCSD implementation for arbitrary high-spin states.

    Herrmann, Nils / Hanrath, Michael

    The Journal of chemical physics

    2021  Volume 156, Issue 5, Page(s) 54111

    Abstract: In this paper, we report on a correctly scaling novel coupled cluster singles and doubles (CCSD) implementation for arbitrary high-spin open-shell states. The chosen cluster operator is completely spin-free, i.e., employs spatial substitutions only. It ... ...

    Abstract In this paper, we report on a correctly scaling novel coupled cluster singles and doubles (CCSD) implementation for arbitrary high-spin open-shell states. The chosen cluster operator is completely spin-free, i.e., employs spatial substitutions only. It is composed of our recently developed Löwdin-type operators [N. Herrmann and M. Hanrath, J. Chem. Phys. 153, 164114 (2020)], which ensure (1) spin completeness and (2) spin adaption, i.e., spin purity of the CC wave function. In contrast to the proof-of-concept matrix-representation-based implementation presented there, the present implementation relies on second quantization and factorized tensor contractions. The generated singles and doubles operators are embedded in an equation generation engine. In the latter, Wick's theorem is used to derive prefactors arising from spin integration directly from the spin-free full contraction patterns. The obtained Wick terms composed of products of Kronecker deltas are represented by special non-antisymmetrized Goldstone diagrams. Identical (redundant) diagrams are identified by solving the underlying graph isomorphism problem. All non-redundant graphs are then automatically translated to locally-one term at a time-factorized tensor contractions. Finally, the spin-adapted and spin-complete (SASC) CCS and CCSD variants are applied to a set of small molecular test systems. Both correlation energies and amplitude norms hint toward a reasonable convergence of the SASC-CCSD method for a Baker-Campbell-Hausdorff series truncation of order four. In comparison to spin orbital CCSD, SASC-CCSD leads to slightly improved correlation energies with differences of up to 1.292mE
    Language English
    Publishing date 2021-12-28
    Publishing country United States
    Document type Journal Article
    ZDB-ID 3113-6
    ISSN 1089-7690 ; 0021-9606
    ISSN (online) 1089-7690
    ISSN 0021-9606
    DOI 10.1063/5.0078020
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Generation of spin-adapted and spin-complete substitution operators for (high spin) open-shell coupled cluster of arbitrary order.

    Herrmann, Nils / Hanrath, Michael

    The Journal of chemical physics

    2020  Volume 153, Issue 16, Page(s) 164114

    Abstract: A rigorous generation of spin-adapted (spin-free) substitution operators for high spin (S = ... ...

    Abstract A rigorous generation of spin-adapted (spin-free) substitution operators for high spin (S = S
    Language English
    Publishing date 2020-10-29
    Publishing country United States
    Document type Journal Article
    ZDB-ID 3113-6
    ISSN 1089-7690 ; 0021-9606
    ISSN (online) 1089-7690
    ISSN 0021-9606
    DOI 10.1063/5.0026762
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Book ; Online: Automatic Routing of Goldstone Diagrams using Genetic Algorithms

    Herrmann, Nils / Hanrath, Michael

    2019  

    Abstract: This paper presents an algorithm for an automatic transformation (=routing) of time ordered topologies of Goldstone diagrams (i.e. Wick contractions) into graphical representations of these topologies. Since there is no hard criterion for an optimal ... ...

    Abstract This paper presents an algorithm for an automatic transformation (=routing) of time ordered topologies of Goldstone diagrams (i.e. Wick contractions) into graphical representations of these topologies. Since there is no hard criterion for an optimal routing, the proposed algorithm minimizes an empirically chosen cost function over a set of parameters. Some of the latter are naturally of discrete type (e.g. interchange of particle/hole lines due to antisymmetry) while others (e.g. x,y-position of nodes) are naturally continuous. In order to arrive at a manageable optimization problem the position space is artificially discretized. In terms of the (i) cost function, (ii) the discrete vertex placement, (iii) the interchange of particle/hole lines the routing problem is now well defined and fully discrete. However, it shows an exponential complexity with the number of vertices suggesting to apply a genetic algorithm for its solution. The presented algorithm is capable of routing non trivial (several loops and crossings) Goldstone diagrams. The resulting diagrams are qualitatively fully equivalent to manually routed ones. The proposed algorithm is successfully applied to several Coupled Cluster approaches and a perturbative (fixpoint iterative) CCSD expansion with repeated diagram substitution.

    Comment: 15 pages, 4 tables, 16 figures
    Keywords Physics - Chemical Physics ; Computer Science - Neural and Evolutionary Computing
    Subject code 000
    Publishing date 2019-06-30
    Publishing country us
    Document type Book ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  4. Book ; Online ; Thesis: Implementation and Application of the Core Polarization Potential Ansatz in Quantum Chemical Systems

    Bubeck, Sascha [Verfasser] / Dolg, Michael [Gutachter] / Hanrath, Michael [Gutachter]

    2021  

    Author's details Sascha Bubeck ; Gutachter: Michael Dolg, Michael Hanrath
    Keywords Naturwissenschaften ; Science
    Subject code sg500
    Language English
    Publisher Universitäts- und Stadtbibliothek Köln
    Publishing place Köln
    Document type Book ; Online ; Thesis
    Database Digital theses on the web

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  5. Article: Higher excitations for an exponential multireference wavefunction Ansatz and single-reference based multireference coupled cluster Ansatz: application to model systems H(4), P(4), and BeH(2).

    Hanrath, Michael

    The Journal of chemical physics

    2008  Volume 128, Issue 15, Page(s) 154118

    Abstract: This article reports on the convergence of the exponential multireference wavefunction Ansatz (MRexpT) [J. Chem. Phys. 123, 84102 (2005)] and the single-reference based multireference coupled cluster Ansatz [J. Chem. Phys. 94, 1229 (1991)] with respect ... ...

    Abstract This article reports on the convergence of the exponential multireference wavefunction Ansatz (MRexpT) [J. Chem. Phys. 123, 84102 (2005)] and the single-reference based multireference coupled cluster Ansatz [J. Chem. Phys. 94, 1229 (1991)] with respect to higher cluster excitations. The approaches are applied to the H(4), P(4), and BeH(2) model systems according to the recently published analysis by Evangelista et al. [J. Chem. Phys. 125, 154113 (2006)]. The results show both MRexpT and SRMRCC to be highly accurate although SRMRCC shows problems due to its lack of Fermi vacuum invariance (symmetry breaking).
    Language English
    Publishing date 2008-04-21
    Publishing country United States
    Document type Journal Article
    ZDB-ID 3113-6
    ISSN 1089-7690 ; 0021-9606
    ISSN (online) 1089-7690
    ISSN 0021-9606
    DOI 10.1063/1.2899645
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: An Efficient Hartree-Fock Implementation Based on the Contraction of Integrals in the Primitive Basis.

    Held, Joseph / Hanrath, Michael / Dolg, Michael

    Journal of chemical theory and computation

    2018  Volume 14, Issue 12, Page(s) 6197–6210

    Abstract: A new approach to implement the restricted closed-shell Hartree-Fock equation is proposed. In the ansatz presented, the explicit transformation of integrals from the primitive to the atomic-orbital basis is omitted. Instead, the density matrix is ... ...

    Abstract A new approach to implement the restricted closed-shell Hartree-Fock equation is proposed. In the ansatz presented, the explicit transformation of integrals from the primitive to the atomic-orbital basis is omitted. Instead, the density matrix is transformed to the primitive basis, in which it is contracted with the untransformed integrals. Obtained is the two-electron part of the Fock matrix, which is transformed back to the atomic orbital basis. The remaining steps of the self-consistent field algorithm are then performed as usual. The program presented here incorporates the most important standard techniques, such as integral prescreening, convergence acceleration (via the direct inversion of the iterative subspace ansatz), and the differential density scheme. Test calculations on standard Hartree-Fock problems were compared to the commercially available MOLPRO and TURBOMOLE program packages. Except in a few special cases, the performance of the program presented here is superior, in comparison to those two programs. Accelerations by up to a factor of 5 were found, with respect to MOLPRO calculations, and up to 3 for TURBOMOLE (in the latter case, up to 55 for generalized contracted basis sets). The program structure is independent of the type of radial contraction; however, the best results are obtained for generalized radial contraction basis sets of low contraction. The program is written in C++ and utilizes code generation engines to automatically generate the routines for the integration and density contraction. Streaming SIMD extensions are used explicitly.
    Language English
    Publishing date 2018-11-09
    Publishing country United States
    Document type Journal Article
    ISSN 1549-9626
    ISSN (online) 1549-9626
    DOI 10.1021/acs.jctc.8b00358
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: An exponential multireference wave-function Ansatz.

    Hanrath, Michael

    The Journal of chemical physics

    2005  Volume 123, Issue 8, Page(s) 84102

    Abstract: An exponential multireference wave-function Ansatz is formulated. In accordance with the state universal coupled-cluster Ansatz of Jeziorski and Monkhorst [Phys. Rev. A 24, 1668 (1981)] the approach uses a reference specific cluster operator. In order to ...

    Abstract An exponential multireference wave-function Ansatz is formulated. In accordance with the state universal coupled-cluster Ansatz of Jeziorski and Monkhorst [Phys. Rev. A 24, 1668 (1981)] the approach uses a reference specific cluster operator. In order to achieve state selectiveness the excitation- and reference-related amplitude indexing of the state universal Ansatz is replaced by an indexing which is based on excited determinants. There is no reference determinant playing a particular role. The approach is size consistent, coincides with traditional single-reference coupled cluster if applied to a single-reference, and converges to full configuration interaction with an increasing cluster operator excitation level. Initial applications on BeH2, CH2, Li2, and nH2 are reported.
    Language English
    Publishing date 2005-08-22
    Publishing country United States
    Document type Journal Article
    ZDB-ID 3113-6
    ISSN 1089-7690 ; 0021-9606
    ISSN (online) 1089-7690
    ISSN 0021-9606
    DOI 10.1063/1.1953407
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Book ; Online ; Thesis: Interpretation of ab initio Calculations of Cerium Compounds and Predictive Power of Density Functional Theory Calculations for Iodine Catalysis

    Mooßen, Oliver [Verfasser] / Dolg, Michael [Gutachter] / Hanrath, Michael [Gutachter]

    2018  

    Author's details Oliver Mooßen ; Gutachter: Michael Dolg, Michael Hanrath
    Keywords Naturwissenschaften ; Science
    Subject code sg500
    Language English
    Publisher Universitäts- und Stadtbibliothek Köln
    Publishing place Köln
    Document type Book ; Online ; Thesis
    Database Digital theses on the web

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  9. Article ; Online: A fully simultaneously optimizing genetic approach to the highly excited coupled-cluster factorization problem.

    Engels-Putzka, Anna / Hanrath, Michael

    The Journal of chemical physics

    2011  Volume 134, Issue 12, Page(s) 124106

    Abstract: In this article we report on the coupled-cluster factorization problem. We describe the first implementation that optimizes (i) the contraction order for each term, (ii) the identification of reusable intermediates, (iii) the selection and factoring out ... ...

    Abstract In this article we report on the coupled-cluster factorization problem. We describe the first implementation that optimizes (i) the contraction order for each term, (ii) the identification of reusable intermediates, (iii) the selection and factoring out of common factors simultaneously, considering all projection levels in a single step. The optimization is achieved by means of a genetic algorithm. Taking a one-term-at-a-time strategy as reference our factorization yields speedups of up to 4 (for intermediate excitation levels, smaller basis sets). We derive a theoretical lower bound for the highest order scaling cost and show that it is met by our implementation. Additionally, we report on the performance of the resulting highly excited coupled-cluster algorithms and find significant improvements with respect to the implementation of Kállay and Surján [J. Chem. Phys. 115, 2945 (2001)] and comparable performance with respect to MOLPRO's handwritten and dedicated open shell coupled cluster with singles and doubles substitutions implementation [P. J. Knowles, C. Hampel, and H.-J. Werner, J. Chem. Phys. 99, 5219 (1993)].
    Language English
    Publishing date 2011-03-28
    Publishing country United States
    Document type Journal Article
    ZDB-ID 3113-6
    ISSN 1089-7690 ; 0021-9606
    ISSN (online) 1089-7690
    ISSN 0021-9606
    DOI 10.1063/1.3561739
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: An efficient matrix-matrix multiplication based antisymmetric tensor contraction engine for general order coupled cluster.

    Hanrath, Michael / Engels-Putzka, Anna

    The Journal of chemical physics

    2010  Volume 133, Issue 6, Page(s) 64108

    Abstract: In this paper, we present an efficient implementation of general tensor contractions, which is part of a new coupled-cluster program. The tensor contractions, used to evaluate the residuals in each coupled-cluster iteration are particularly important for ...

    Abstract In this paper, we present an efficient implementation of general tensor contractions, which is part of a new coupled-cluster program. The tensor contractions, used to evaluate the residuals in each coupled-cluster iteration are particularly important for the performance of the program. We developed a generic procedure, which carries out contractions of two tensors irrespective of their explicit structure. It can handle coupled-cluster-type expressions of arbitrary excitation level. To make the contraction efficient without loosing flexibility, we use a three-step procedure. First, the data contained in the tensors are rearranged into matrices, then a matrix-matrix multiplication is performed, and finally the result is backtransformed to a tensor. The current implementation is significantly more efficient than previous ones capable of treating arbitrary high excitations.
    Language English
    Publishing date 2010-08-14
    Publishing country United States
    Document type Journal Article
    ZDB-ID 3113-6
    ISSN 1089-7690 ; 0021-9606
    ISSN (online) 1089-7690
    ISSN 0021-9606
    DOI 10.1063/1.3467878
    Database MEDical Literature Analysis and Retrieval System OnLINE

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