TY - JOUR A1 - Kramer, Tobias A1 - Noack, Matthias A1 - Reinefeld, Alexander A1 - Rodríguez, Mirta A1 - Zelinskyi, Yaroslav T1 - Efficient calculation of open quantum system dynamics and time-resolved spectroscopy with Distributed Memory HEOM (DM-HEOM) JF - Journal of Computational Chemistry N2 - Time- and frequency resolved optical signals provide insights into the properties of light harvesting molecular complexes, including excitation energies, dipole strengths and orientations, as well as in the exciton energy flow through the complex. The hierarchical equations of motion (HEOM) provide a unifying theory, which allows one to study the combined effects of system-environment dissipation and non-Markovian memory without making restrictive assumptions about weak or strong couplings or separability of vibrational and electronic degrees of freedom. With increasing system size the exact solution of the open quantum system dynamics requires memory and compute resources beyond a single compute node. To overcome this barrier, we developed a scalable variant of HEOM. Our distributed memory HEOM, DM-HEOM, is a universal tool for open quantum system dynamics. It is used to accurately compute all experimentally accessible time- and frequency resolved processes in light harvesting molecular complexes with arbitrary system-environment couplings for a wide range of temperatures and complex sizes. Y1 - 2018 U6 - https://doi.org/doi:10.1002/jcc.25354 VL - 39 IS - 22 SP - 1779 EP - 1794 PB - Wiley Periodicals, Inc. ER - TY - JOUR A1 - Kramer, Tobias A1 - Noack, Matthias A1 - Reimers, Jeffrey R. A1 - Reinefeld, Alexander A1 - Rodríguez, Mirta A1 - Yin, Shiwei T1 - Energy flow in the Photosystem I supercomplex: comparison of approximative theories with DM-HEOM JF - Chemical Physics N2 - We analyze the exciton dynamics in PhotosystemI from Thermosynechococcus elongatus using the distributed memory implementation of the hierarchical equation of motion (DM-HEOM) for the 96 Chlorophylls in the monomeric unit. The exciton-system parameters are taken from a first principles calculation. A comparison of the exact results with Foerster rates and Markovian approximations allows one to validate the exciton transfer times within the complex and to identify deviations from approximative theories. We show the optical absorption, linear, and circular dichroism spectra obtained with DM-HEOM and compare them to experimental results. Y1 - 2018 U6 - https://doi.org/10.1016/j.chemphys.2018.05.028 VL - 515 SP - 262 EP - 271 PB - Elsevier B.V. ER -