Ultrafast Long-Range Charge Separation in Organic Semiconductor Photovoltaic Diodes

Simon Gélinas, Akshay Rao, Abhishek Kumar, Samuel Smith, Alex W. Chin, Jenny Clark, Tom S. van der Poll, Guillermo C. Bazan, Richard H. Friend

19th International Conference on Ultrafast Phenomena · 2014 · 33 citations · 3 references

Concepts

TL;DR

In photovoltaic devices, efficient separation of photoexcited electrons and holes across the junction is essential to avoid recombination and generate current. Ultrafast spectroscopy of thiophene–fullerene systems revealed charge separation rates far exceeding diffusion limits, suggesting a coherent delocalization mechanism involving fullerene π‑states. Gélinas et al.

Abstract

Early Separation In photovoltaic devices, electrons excited by the absorption of light must travel across a junction, while the positively charged “holes” they leave behind effectively migrate in the opposite direction. If the electrons and holes do not separate efficiently, they can recombine and fail to produce any appreciable current. Gélinas et al. (p. 512 , published online 12 December; see the Perspective by Bredas ) studied this separation process by ultrafast optical absorption spectroscopy in thiophene-derived donor-fullerene acceptor systems common in organic photovoltaics and report a rate significantly faster than simple charge diffusion would suggest. The results implicate a coherent charge delocalization process, likely to involve fullerene π-electron states.

References

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