TY - JOUR
T1 - Impact of Nonfullerene Acceptor Side Chain Variation on Transistor Mobility
AU - Bristow, Helen
AU - Thorley, Karl J.
AU - White, Andrew J. P.
AU - Wadsworth, Andrew
AU - Babics, Maxime
AU - Hamid, Zeinab
AU - Zhang, Weimin
AU - Paterson, Alexandra
AU - Kosco, Jan
AU - Panidi, Julianna
AU - Anthopoulos, Thomas D.
AU - McCulloch, Iain
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledgements: The authors thank KAUST and Eight19 for financial support. They also acknowledge EC FP7 Project SC2 (610115), EC H2020 (643791), EPSRC Projects EP/G037515/1, EP/M005143/1, EP/L016702/1 as well as NSF DMREF program DMREF-1627428.
PY - 2019/7/23
Y1 - 2019/7/23
N2 - Organic photovoltaic power conversion efficiencies exceeding 14% can largely be attributed to the development of nonfullerene acceptors (NFAs). Many of these molecules are structural derivatives of IDTBR and ITIC, two common NFAs. By modifying the chemical structure of the acceptor, the optical absorption, energy levels, and bulk heterojunction morphology can be tuned. However, the effect of structural modifications on NFA charge transport properties has not yet been fully explored. In this work, the relationship between chemical structure, molecular packing, and charge transport, as measured in organic thin-film transistors (OTFTs), is investigated for two high performance NFAs, namely O-IDTBR and ITIC, along with their structural derivatives EH-IDTBR and ITIC-Th. O-IDTBR exhibits a higher n-type saturation field effect mobility of 0.12 cm2 V−1 s−1 compared with the other acceptors investigated. This can be attributed to the linear side chains of O-IDTBR which direct an interdigitated columnar packing motif. The study provides insight into the transport properties and molecular packing of NFAs, thereby contributing to understanding the relationship between chemical structure, material properties, and device performance for these materials. The high electron mobility achieved by O-IDTBR also suggests its applications can be extended to use as an n-type semiconductor in OTFTs.
AB - Organic photovoltaic power conversion efficiencies exceeding 14% can largely be attributed to the development of nonfullerene acceptors (NFAs). Many of these molecules are structural derivatives of IDTBR and ITIC, two common NFAs. By modifying the chemical structure of the acceptor, the optical absorption, energy levels, and bulk heterojunction morphology can be tuned. However, the effect of structural modifications on NFA charge transport properties has not yet been fully explored. In this work, the relationship between chemical structure, molecular packing, and charge transport, as measured in organic thin-film transistors (OTFTs), is investigated for two high performance NFAs, namely O-IDTBR and ITIC, along with their structural derivatives EH-IDTBR and ITIC-Th. O-IDTBR exhibits a higher n-type saturation field effect mobility of 0.12 cm2 V−1 s−1 compared with the other acceptors investigated. This can be attributed to the linear side chains of O-IDTBR which direct an interdigitated columnar packing motif. The study provides insight into the transport properties and molecular packing of NFAs, thereby contributing to understanding the relationship between chemical structure, material properties, and device performance for these materials. The high electron mobility achieved by O-IDTBR also suggests its applications can be extended to use as an n-type semiconductor in OTFTs.
UR - http://hdl.handle.net/10754/656275
UR - https://onlinelibrary.wiley.com/doi/abs/10.1002/aelm.201900344
UR - http://www.scopus.com/inward/record.url?scp=85069871735&partnerID=8YFLogxK
U2 - 10.1002/aelm.201900344
DO - 10.1002/aelm.201900344
M3 - Article
VL - 5
SP - 1900344
JO - Advanced Electronic Materials
JF - Advanced Electronic Materials
SN - 2199-160X
IS - 10
ER -