We review recent work employing high-dimensional quantum dynamical techniques to study ultrafast charge separation in functional organic materials, in view of understanding the key microscopic factors that lead to efficient charge generation in photovoltaics applications. As highlighted by recent experiments, these processes can be guided by quantum coherence, despite the presence of static and dynamic disorder. The present approach combines first-principles parametrized lattice Hamiltonians, based on Time-Dependent Density Functional Theory (TDDFT) and/or high-level electronic structure calculations, with accurate quantum dynamics simulations using the Multi-Configuration Time-Dependent Hartree (MCTDH) method. This contribution specifically addresses the mechanism of charge generation in (i) regioregular oligothiophene-fullerene aggregates, and (ii) highly ordered oligothiophene-perylene diimide co-oligomer assemblies. These studies highlight that chemical design of donor-acceptor combinations needs to account for the effects of electronic delocalization and the modified energetics due to molecular packing, as well as multiple transfer pathways and internal conversion channels induced by vibronic interactions.excitonic states, molecular packing, organic photovoltaics, quantum dynamics, ultrafast charge separation
| I N TR ODU C TI ONIn organic donor-acceptor (DA) materials developed for photovoltaics applications, the break-up of photogenerated excitons at DA heterojunction interfaces initiates the irreversible separation of charge carriers. [1,2] Over the past few years, it has become increasingly clear that the efficiency of this process depends on a complex interplay of different factors, such that design principles based on the engineering of molecular structure and DA band offsets are not necessarily sufficient. Indeed, the photochemical processes inherent to the molecular donor and acceptor materials necessitate a molecular-level analysis that may deviate from the basic picture derived from semiconductor physics. This is underscored by an increasing body of evidence from time-resolved spectroscopies [3][4][5][6][7] showing that the elementary energy and charge transfer (CT) processes in typical photovoltaic materials are often of quantum coherent character. Conventional kinetic descriptions are therefore not apt to render a faithful picture of these elementary steps, and may only be valid on longer time scales where hopping type transport dynamics sets in.Even long-range electron-hole separation under the effect of a Coulomb barrier may not necessarily obey the slow, thermally activated dynamics described by the Onsager-Braun model. [8] Indeed, recent time-resolved experiments, for example, for prototypical blends of poly-3-hexylthiophene (P3HT) and the fullerene derivative [6,6]-phenyl-C 61 butyric acid methyl ester (PCBM) and related systems, report ultrafast longrange charge separation, especially in materials exhibiting regioregular morphologies. [9][10][11][12][13][14][15] To explain these ob...