Issue 10, 2016

A non-fullerene electron acceptor modified by thiophene-2-carbonitrile for solution-processed organic solar cells

Abstract

Effective electron acceptor materials usually have a deep lowest unoccupied molecular orbital (LUMO) energy level that can split excitons and generate current. A non-fullerene electron acceptor (F8-DPPTCN) was developed, using fluorene as the core with arms of diketopyrrolopyrrole (DPP) having thiophene-2-carbonitrile as the terminal units. The new molecule had a LUMO of −3.65 eV and a narrow bandgap (Eg) of 1.66 eV, owing to the electronegativity of the thiophene-2-carbonitrile group and its conjugation with DPP units. Organic solar cells (OSCs) with F8-DPPTCN as the acceptor and poly(3-hexylthiophene) (P3HT) as the donor were fabricated. A power conversion efficiency (PCE) of 2.37% was obtained with an open-circuit voltage (Voc) of 0.97 V, a short-circuit current (Jsc) of 6.25 mA cm−2, and a fill factor (FF) of 0.39. Structural characterization showed that P3HT and F8-DPPTCN were kinetically trapped in a weakly separated state whereas thermal annealing led to the crystallization of P3HT and the formation of a network structure with a mesh-size of several hundred nanometers. When a solvent additive, diiodooctane, was used and the mixture was thermally annealed, both P3HT and F8-DPPTCN crystallized and a multi-length scale network was formed. Though the PCEs were low, the changes in the PCE could be correlated with the morphological changes, opening pathways to increase performance further.

Graphical abstract: A non-fullerene electron acceptor modified by thiophene-2-carbonitrile for solution-processed organic solar cells

Supplementary files

Article information

Article type
Paper
Submitted
04 Sun 2016
Accepted
03 Yan 2016
First published
04 Yan 2016

J. Mater. Chem. A, 2016,4, 3777-3783

A non-fullerene electron acceptor modified by thiophene-2-carbonitrile for solution-processed organic solar cells

S. Li, J. Yan, C. Li, F. Liu, M. Shi, H. Chen and T. P. Russell, J. Mater. Chem. A, 2016, 4, 3777 DOI: 10.1039/C6TA00056H

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