TY - JOUR
T1 - Water/Ethanol Soluble p-Type Conjugated Polymers for the Use in Organic Photovoltaics
AU - Pan, Xun
AU - Sharma, Anirudh
AU - Kroon, Renee
AU - Gedefaw, Desta
AU - Elmas, Sait
AU - Yin, Yanting
AU - Andersson, Gunther G.
AU - Lewis, David A.
AU - Andersson, Mats R.
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledgements: The authors thank the Flinders University for financial support. This research was supported by the Australian Research Council’s Discovery Projects funding scheme (Projects DP170102467 and DP160102356). The facilities at Flinders University are supported by the Australian Nano Fabrication Facility (ANFF) and the Flinders Microscopy and Microanalysis (FMMA), which are gratefully acknowledged. Special thanks to Qian Li from the Key Laboratory of High Performance Polymer Materials and Technology of Ministry of Education, Nanjing University for the great help with GPC measurements. Funding. This research was supported by the Australian Research Council’s Discovery Projects funding scheme (Projects DP170102467 and DP160102356).
PY - 2020/8/14
Y1 - 2020/8/14
N2 - We have developed two series of p-type conjugated polymers based on poly[2,3-bis-(3-octyloxyphenyl)quinoxaline-5,8-diyl-alt-thiophene-2,5-diyl] (TQ1) polymeric backbone utilizing polar pendant groups, i.e., tertiary amine and pyridine, to achieve switchable solubility in water and ethanol. By balancing the ratio between polar and non-polar side-groups, we could combine green-solvent processability with the manufacturing of functional photovoltaic devices. Due to the unavailability of water/alcohol soluble acceptors, the photovoltaic performance of these new polymers was evaluated using organic solvent by incorporating PC61BM. For water/alcohol soluble partial amine-based polymers, we achieve a maximum power conversion efficiency (PCE) of ∼0.8% whereas alcohol soluble partial pyridine-based polymers show enhanced PCE of ∼1.3% with inverted device structure. We propose that the enhancement in PCE is a result of the reduction in amino-group content and the lower basicity of pyridine, both of which decrease the interaction between functionalized polymers with the anode interface material and reduce the miscibility of the donor and acceptor. Further improvement of the photovoltaic performance, in particular the open-circuit voltage (Voc), was achieved by using an anode buffer layer to mitigate the unfavorable interaction of the amino/pyridine groups with the MoO3 electrode. Our work demonstrated the possibility of substituent modification for conjugated polymers using tertiary amine and pyridine groups to achieve water/alcohol soluble and functional donor materials.
AB - We have developed two series of p-type conjugated polymers based on poly[2,3-bis-(3-octyloxyphenyl)quinoxaline-5,8-diyl-alt-thiophene-2,5-diyl] (TQ1) polymeric backbone utilizing polar pendant groups, i.e., tertiary amine and pyridine, to achieve switchable solubility in water and ethanol. By balancing the ratio between polar and non-polar side-groups, we could combine green-solvent processability with the manufacturing of functional photovoltaic devices. Due to the unavailability of water/alcohol soluble acceptors, the photovoltaic performance of these new polymers was evaluated using organic solvent by incorporating PC61BM. For water/alcohol soluble partial amine-based polymers, we achieve a maximum power conversion efficiency (PCE) of ∼0.8% whereas alcohol soluble partial pyridine-based polymers show enhanced PCE of ∼1.3% with inverted device structure. We propose that the enhancement in PCE is a result of the reduction in amino-group content and the lower basicity of pyridine, both of which decrease the interaction between functionalized polymers with the anode interface material and reduce the miscibility of the donor and acceptor. Further improvement of the photovoltaic performance, in particular the open-circuit voltage (Voc), was achieved by using an anode buffer layer to mitigate the unfavorable interaction of the amino/pyridine groups with the MoO3 electrode. Our work demonstrated the possibility of substituent modification for conjugated polymers using tertiary amine and pyridine groups to achieve water/alcohol soluble and functional donor materials.
UR - http://hdl.handle.net/10754/665044
UR - https://www.frontiersin.org/article/10.3389/fmats.2020.00281/full
UR - http://www.scopus.com/inward/record.url?scp=85090006689&partnerID=8YFLogxK
U2 - 10.3389/fmats.2020.00281
DO - 10.3389/fmats.2020.00281
M3 - Article
SN - 2296-8016
VL - 7
JO - Frontiers in Materials
JF - Frontiers in Materials
ER -