Enhancement of Vibronic and Ground-State Vibrational Coherences in 2D Spectra of Photosynthetic Complexes
arXiv:1211.4397 · doi:10.1038/srep02029
Abstract
A vibronic-exciton model is applied to investigate the mechanism of enhancement of coherent oscillations due to mixing of electronic and nuclear degrees of freedom recently proposed as the origin of the long-lived oscillations in 2D spectra of the FMO complex [Christensson et al. J. Phys. Chem. B 116 (2012) 7449]. We reduce the problem to a model BChl dimer to elucidate the role of resonance coupling, site energies, nuclear mode and energy disorder in the enhancement of vibronic-exciton and ground-state vibrational coherences, and to identify regimes where this enhancement is significant. For a heterodimer representing the two coupled BChls 3 and 4 of the FMO complex, the initial amplitude of the vibronic-exciton and vibrational coherences are enhanced by up to 15 and 5 times, respectively, compared to the vibrational coherences in the isolated monomer. This maximum initial amplitude enhancement occurs when there is a resonance between the electronic energy gap and the frequency of the vibrational mode. The bandwidth of this enhancement is about 100 cm-1 for both mechanisms. The excitonic mixing of electronic and vibrational DOF leads to additional dephasing relative to the vibrational coherences. We evaluate the dephasing dynamics by solving the quantum master equation in Markovian approximation and observe a strong dependence of the life-time enhancement on the mode frequency. Long-lived vibronic-exciton coherences are found to be generated only when the frequency of the mode is in the vicinity of the electronic resonance. Although the vibronic-exciton coherences exhibit a larger initial amplitude compared to the ground-state vibrational coherences, we conclude that both type have a similar magnitude at long time for the present model. The ability to distinguish between vibronic-exciton and ground-state vibrational coherences in the general case of molecular aggregate is discussed.
16 pages, 6 figures
References in corpus (8)
- Environment-Assisted Quantum Transport
- Origin of Long Lived Coherences in Light-Harvesting Complexes
- Vibrational vs. electronic coherences in 2D spectrum of molecular systems
- The fundamental role of quantized vibrations in coherent light harvesting by cryptophyte algae
- Long-Lived Electronic Coherence in Dissipative Exciton-Dynamics of Light-Harvesting Complexes
- Incoherent Excitation of Thermally Equilibrated Open Quantum Systems
- A witness for coherent electronic oscillations in ultrafast spectroscopy
- The nature of the low energy band of the Fenna-Matthews-Olson complex: vibronic signatures
Cited by in corpus (35)
- Origin of long-lived oscillations in 2D-spectra of a Quantum Vibronic Model: Electronic vs Vibrational coherence
- Energy transfer in structured and unstructured environments: master equations beyond the Born-Markov approximations
- Distinctive character of electronic and vibrational coherences in disordered molecular aggregates
- Multi-Layer Multi-Configuration Time-Dependent Hartree (ML-MCTDH) Approach to the Correlated Exciton-Vibrational Dynamics in the FMO Complex
- Impact of environmentally induced fluctuations on quantum mechanically mixed electronic and vibrational pigment states in photosynthetic energy transfer and 2D electronic spectra
- Vibronic phenomena and exciton-vibrational interference in two-dimensional spectra of molecular aggregates
- Atomistic study of energy funneling in the light-harvesting complex of green sulfur bacteria
- Disentangling electronic and vibronic coherences in two-dimensional echo spectra
- Vibronic resonances facilitate excited state coherence in light harvesting proteins at room temperature
- Vibronic coupling explains the ultrafast carotenoid-to-bacteriochlorophyll energy transfer in natural and artificial light harvesters
- Explicit Correlated Exciton-Vibrational Dynamics of the FMO Complex
- Hidden Vibronic and Excitonic Structure and Vibronic Coherence Transfer in the Bacterial Reaction Center
- Exact Simulation of Pigment-Protein Complexes Unveils Vibronic Renormalization of Electronic Parameters in Ultrafast Spectroscopy
- Vibration-assisted resonance in photosynthetic excitation energy transfer
- Coherence and population dynamics of chlorophyll excitations in FCP complex: Two-dimensional spectroscopy study
- The hierarchical and perturbative forms of stochastic Schrödinger equations and their applications to carrier dynamics in organic materials
- Disentangling electronic and vibrational coherence in the Phycocyanin-645 light-harvesting complex
- Exciton coupling induces vibronic hyperchromism in light-harvesting complexes
- On the theory of excitonic delocalization for robust vibronic dynamics in LH2
- Dynamic Coherence in Excitonic Molecular Complexes under Various Excitation Conditions
- Systematic coarse-graining of environments for the non-perturbative simulation of open quantum systems
- Rerouting Excitation Transfer in the Fenna-Matthews-Olson Complex
- Treatment of Herzberg-Teller and non-Condon effects in optical spectra with Hierarchical Equations of Motion
- Dissipation enhanced vibrational sensing in an olfactory molecular switch
- Practical Witness for Electronic Coherences
- Cooperative subwavelength molecular quantum emitter arrays
- Optical Activity from the Exciton Aharonov-Bohm Effect: A Floquet Engineering Approach
- Transfer of Vibrational Coherence Through Incoherent Energy Transfer Process in Förster Limi
- Signatures of spatially correlated noise and non-secular effects in two-dimensional electronic spectroscopy
- Multi-color quantum control for suppressing ground state coherences in two-dimensional electronic spectroscopy
- Coherence and its Role in Excitation Energy Transfer in Fenna-Mathews-Olson Complex
- Simulations of coherent nonlinear optical response of molecular vibronic dimers
- Nonadiabatic Sunlight-harvesting
- Observation of Coherence in the Photosystem II Reaction Center
- Self-consistent approach to the dynamics of excitation energy transfer in multichromophoric systems