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Erling Thyrhaug

Publications and source records attributed to Erling Thyrhaug.

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Broadband shot-to-shot transient absorption anisotropy

Transient absorption (TA) is the most widespread method to follow ultrafast dynamics in molecules and materials. The related method of TA anisotropy (TAA) reports on the ultrafast reorientation dynamics of transition dipole moments, reporting on phenomena ranging from electronic dephasing to orientational diffusion. While these are fundamental aspects complementary to TA, TAA is generally less widely used. The main reason is that TAA signals are usually not measured directly but are retrieved from two consecutive TA measurements with parallel and perpendicular polarization of pump and probe pulses. This means that even minor systematic errors in these measurements lead to drastic changes in the TAA signal. In this work, the authors demonstrate alternating shot-to-shot detection of TA measurements with different pump polarization, minimizing systematic errors due to laser fluctuations. The employed broadband detection lets us discuss effects dependent on detection wavelength in the ultrafast anisotropy decay of 2,3-Naphthalocyanin, a system previously scrutinized by David Jonas and co-workers. In particular we compare timescales of population relaxation and decoherence and supported the proposals for isotropic type of relaxation in square symmetric molecules.

physics.optics

Model-Independent Simulation Complexity of Complex Quantum Dynamics

We present a model-independent measure of dynamical complexity based on simulating complex quantum dynamics using stroboscopic Markovian dynamics. Tools from classical signal processing enable us to infer the Hilbert space dimension of a complex quantum system evolving under a time-independent Hamiltonian via pulsed interrogation. We evaluate our model-independent simulation complexity (MISC) for the spin-boson model and simulated third-order pump-probe spectroscopy data for exciton transport in coupled dimers with vibrational levels. The former provides insights into coherence and population dynamics in the two-level system while the latter reveals the dimension of the singly-excited manifold of the dimer. Finally, we probe the complexity of excitonic transport in light harvesting 2 (LH2) and Fenna-Matthews-Olson (FMO) complexes using data from two recent nonlinear ultrafast optical spectroscopy experiments. For the latter we make some model-independent inferences that are commensurate with model-specific ones. This includes estimating the fewest number of parameters needed to fit the experimental data and identifying the spatial extent, i.e., delocalization size, of quantum states occurring in this complex quantum dynamics.

quant-ph

Unravelling coherences in the FMO complex

The idea that excitonic state (electronic) coherences are of fundamental importance to natural photosynthesis gained popularity when, a decade ago, slowly dephasing quantum beats were observed in the two-dimensional electronic spectra of the Fenna-Matthews-Olson complex at 77 K. These were assigned to quantum superpositions of excitonic states; a controversial interpretation, as the spectral linewidths suggested fast dephasing arising from strong interactions with the environment. While it has been pointed out that vibrational motion produces similar spectral signatures, concrete assignment of these coherences to distinct physical processes is still lacking. Here we revisit the coherence dynamics of the Fenna-Matthews-Olson complex using polarization-controlled two-dimensional electronic spectroscopy, supported by theoretical modelling. We show that the long-lived quantum beats originate exclusively from vibrational coherences, whereas electronic coherences dephase entirely within 240 fs even at 77 K - a timescale too short to play a significant role in light harvesting. Additionally, we demonstrate that specific vibrational coherences are excited via vibronically coupled states. The detection of vibronic coupling indicates the relevance of this phenomenon for photosynthetic energy transfer.

physics.chem-ph