Abstract

Photo-induced charge transfer at molecular heterojunctions has gained particular interest due to the development of organic solar cells (OSC) based on blends of electron donating and accepting materials. While charge transfer between donor and acceptor molecules can be described by Marcus theory, additional carrier delocalization and coherent propagation might play the dominant role. Here, we describe ultrafast charge separation at the interface of a conjugated polymer and an aggregate of the fullerene derivative PCBM using the stochastic Schrödinger equation (SSE) and reveal the complex time evolution of electron transfer, mediated by electronic coherence and delocalization. By fitting the model to ultrafast charge separation experiments, we estimate the extent of electron delocalization and establish the transition from coherent electron propagation to incoherent hopping. Our results indicate that even a relatively weak coupling between PCBM molecules is sufficient to facilitate electron delocalization and efficient charge separation at organic interfaces.

Highlights

  • Wide range of intermolecular couplings, leading to different charge separation scenarios

  • All of them lead to charge separation kinetics which qualitatively agree with experimental results

  • Our results show that the electron is transferred from the donor site to a nearby pool of coherently coupled acceptor sites within ~300 fs

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Summary

Introduction

Wide range of intermolecular couplings, leading to different charge separation scenarios. We set simulation parameters typical for polymer-PCBM solar cells (see Supplementary Information), we find that the most important parameter governing the coherent (

Results
Conclusion
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