Skip to main content
European Commission logo print header

Energy and charge transfer nonadiabatic dynamics in light-harvesting molecules and nanostructures

Project description

Creating light-induced nonadiabatic process simulations

Nonadiabatic dynamics is a crucial aspect of nuclear science that holds great promise for the field’s future. However, the current methods used to simulate light-induced nonadiabatic processes are inefficient and hamper progress. Funded by the European Research Council, the DYNAMO project seeks to address this challenge by developing a new methodology for simulating nonadiabatic processes induced by light in multichromophoric light-harvesting assemblies. Researchers aim to use mixed quantum-classical methods to improve simulation efficiency significantly. The ultimate goal is to evaluate energy and charge transport dynamics in new light-harvesting systems using the results obtained from these simulations.


The goal of DYNAMO is to develop an efficient mixed quantum-classical methodology for the simulation of light-induced nonadiabatic processes in multichromophoric light-harvesting assemblies and to apply it to explore energy and charge transport dynamics in novel classes of light-harvesting systems. There is growing evidence that nonadiabatic relaxation processes play a fundamental role in determining the efficiency of the excitonic transfer or charge injection. In addition to the intramolecular nonradiative transitions through conical intersections, well known from photochemistry, the coupling between the chromophores in multichromophoric assemblies gives rise to novel intermolecular nonadiabatic relaxation channels through funnels between the delocalized excitonic and/or charge transfer states. In order to simulate coupled electron-nuclear dynamics in multichromophoric nanostructures we will develop and implement light-induced surface hopping methods and combine them with efficient electronic structure methods. For a unified description of excitonic and charge transfer states we will combine constrained density functional theory (CDFT) and linear response time-resolved density functional theory (TDDFT) within the configuration interaction framework. The direct link with the experiment will be provided through the simulation of time-resolved multidimensional spectra in the mixed quantum-classical framework. We will apply the new methodology to investigate energy and charge transport in nanostructures of self-assembled organic molecules (e.g. tubular J-aggregates), in low band-gap organic polymers (e.g. squaraines) and in hybrid plasmon-exciton architectures, where the photon capture and charge injection efficiency can be enhanced by the interaction with plasmonic fields. The ultimate goal is to reveal mechanisms of efficient energy and charge transfer using a first principles methodology, providing guidance for the design of efficient light-harvesting systems.

Host institution

Net EU contribution
€ 1 501 187,50
97070 Wuerzburg

See on map

Bayern Unterfranken Würzburg, Kreisfreie Stadt
Activity type
Higher or Secondary Education Establishments
Total cost
€ 1 501 187,50

Beneficiaries (1)