Atomistic non-adiabatic dynamics of the LH2 complex with a GPU-accelerated ab initio exciton model

Aaron Sisto, Marc Van der Kamp, Clem Stross, Michael O'Connor, Simon McIntosh-Smith, Graham T. Johnson, Edward G. Hohenstein, Fred Manby, David Glowacki*, Todd Martinez

*Corresponding author for this work

Research output: Contribution to journalArticle (Academic Journal)peer-review

56 Citations (Scopus)
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We recently outlined an efficient multi-tiered parallel ab initio excitonic framework that utilizes time dependent density functional theory (TDDFT) to calculate ground and excited state energies and gradients of large supramolecular complexes in atomistic detail – enabling us to undertake nonadiabatic simulations which explicitly account for the coupled anharmonic vibrational motion of all the constituent atoms in a supramolecular system. Here we apply that framework to the 27 coupled bacterio-cholorophyll-a chromophores which make up the LH2 complex, using it to compute an onthe-fly nonadiabatic surface-hopping (SH) trajectory of electronically excited LH2. Part one of this article is focussed on calibrating our ab initio exciton Hamiltonian using two key parameters: a shift δ, which corrects for the error in TDDFT vertical excitation energies; and an effective dielectric constant ε, which describes the average screening of the transition-dipole coupling between
chromophores. Using snapshots obtained from equilibrium molecular dynamics simulations (MD) of LH2, we tune the values of both δ and ε through fitting to the thermally broadened experimental absorption spectrum, giving a linear absorption spectrum that agrees reasonably well with experiment. In the part two of this article, we construct a time-resolved picture of the coupled
vibrational and excitation energy transfer (EET) dynamics in the sub-picosecond regime following photo-excitation. Assuming Franck-Condon excitation of a narrow eigenstate band centred at 800 nm, we use surface hopping to follow a single nonadiabatic dynamics trajectory within the full eigenstate manifold. Consistent with experimental data, this trajectory gives timescales for
B800 → B850 population transfer (τ B800→B850 ) between 650 – 1050 fs, and B800 population decay ( τ 800→ ) between 10 – 50 fs. The dynamical picture that emerges is one of rapidly fluctuating LH2 eigenstates that are delocalized over multiple chromophores and undergo frequent crossing on a femtosecond timescale as a result of the atomic vibrations of the constituent chromophores. The eigenstate fluctuations arise from disorder that is driven by vibrational dynamics with multiple characteristic timescales. The scalability of our ab initio excitonic computational framework across massively parallel architectures opens up the possibility of addressing a wide range of questions, including how specific dynamical motions impact both the pathways and efficiency of electronic
energy-transfer within large supramolecular systems.
Original languageEnglish
Pages (from-to)14924-14936
Number of pages13
JournalPhysical Chemistry Chemical Physics
Issue number23
Early online date28 Mar 2017
Publication statusPublished - 21 Jun 2017


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