New Generation Hole Transporting Materials for Perovskite Solar Cells
Amide-Based Small-Molecules with Nonconjugated Backbones
Michiel L. Petrus (Ludwig Maximilians University)
Kelly Schutt (University of Oxford)
Maximilian T. Sirtl (Ludwig Maximilians University)
Eline Hutter (TU Delft - ChemE/Opto-electronic Materials)
Anna C. Closs (Ludwig Maximilians University)
James M. Ball (Istituto Italiano di Tecnologia)
Johan Bijleveld (Istituto Italiano di Tecnologia)
Annamaria Petrozza (Istituto Italiano di Tecnologia)
Thomas Bein (Ludwig Maximilians University)
T.J. Dingemans (University of North Carolina)
Tom Savenije (TU Delft - ChemE/Opto-electronic Materials)
Henry Snaith (University of Oxford)
Pablo Docampo (Newcastle University)
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Abstract
State-of-the-art perovskite-based solar cells employ expensive, organic hole transporting materials (HTMs) such as Spiro-OMeTAD that, in turn, limits the commercialization of this promising technology. Herein an HTM (EDOT-Amide-TPA) is reported in which a functional amide-based backbone is introduced, which allows this material to be synthesized in a simple condensation reaction with an estimated cost of <$5 g−1. When employed in perovskite solar cells, EDOT-Amide-TPA demonstrates stabilized power conversion efficiencies up to 20.0% and reproducibly outperforms Spiro-OMeTAD in direct comparisons. Time resolved microwave conductivity measurements indicate that the observed improvement originates from a faster hole injection rate from the perovskite to EDOT-Amide-TPA. Additionally, the devices exhibit an improved lifetime, which is assigned to the coordination of the amide bond to the Li-additive, offering a novel strategy to hamper the migration of additives. It is shown that, despite the lack of a conjugated backbone, the amide-based HTM can outperform state-of-the-art HTMs at a fraction of the cost, thereby providing a novel set of design strategies to develop new, low-cost HTMs.
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