Molecular helices as electron acceptors in high-performance bulk heterojunction solar cells

Yu Zhong(Columbia University), M. Tuan Trinh(Columbia University), Rongsheng Chen(Wuhan University of Science and Technology), Geoffrey E. Purdum(Princeton University), Petr P. Khlyabich(Princeton University), Melda Sezen-Edmonds(Princeton University), Seokjoon Oh(Columbia University), Haiming Zhu(Columbia University), Brandon Fowler(Columbia University), Boyuan Zhang(Columbia University), Wei Wang(Columbia University), Chang‐Yong Nam(Brookhaven National Laboratory), Matthew Y. Sfeir(Brookhaven National Laboratory), Charles T. Black(Brookhaven National Laboratory), Michael L. Steigerwald(Columbia University), Yueh‐Lin Loo(Princeton University), Fay Ng(Columbia University), Xiaolei Zhu(Columbia University), Colin Nuckolls(Columbia University)
Nature Communications
September 18, 2015
Cited by 566Open Access
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Abstract

Despite numerous organic semiconducting materials synthesized for organic photovoltaics in the past decade, fullerenes are widely used as electron acceptors in highly efficient bulk-heterojunction solar cells. None of the non-fullerene bulk heterojunction solar cells have achieved efficiencies as high as fullerene-based solar cells. Design principles for fullerene-free acceptors remain unclear in the field. Here we report examples of helical molecular semiconductors as electron acceptors that are on par with fullerene derivatives in efficient solar cells. We achieved an 8.3% power conversion efficiency in a solar cell, which is a record high for non-fullerene bulk heterojunctions. Femtosecond transient absorption spectroscopy revealed both electron and hole transfer processes at the donor-acceptor interfaces. Atomic force microscopy reveals a mesh-like network of acceptors with pores that are tens of nanometres in diameter for efficient exciton separation and charge transport. This study describes a new motif for designing highly efficient acceptors for organic solar cells.


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