Source abstract
Abstract
High Resolution Image Download MS PowerPoint Slide Eco-friendly solution processing and the low-cost synthesis of photoactive materials are important requirements for the commercialization of organic solar cells (OSCs). Although varieties of aqueous-soluble acceptors have been developed, the availability of aqueous-processable polymer donors remains quite limited. In particular, the generally shallow highest occupied molecular orbital (HOMO) energy levels of existing polymer donors limit further increases in the power conversion efficiency (PCE). Here, we design and synthesize two water/alcohol-processable polymer donors, poly[(thiophene-2,5-diyl)- alt -(2-((13-(2,5,8,11-tetraoxadodecyl)-2,5,8,11-tetraoxatetradecan-14-yl)oxy)-6,7-difluoroquinoxaline-5,8-diyl)] (P(Qx8O-T) ) and poly[(selenophene-2,5-diyl)- alt -(2-((13-(2,5,8,11-tetraoxadodecyl)-2,5,8,11-tetraoxatetradecan-14-yl)oxy)-6,7-difluoroquinoxaline-5,8-diyl)] ( P(Qx8O-Se) ) with oligo(ethylene glycol) (OEG) side chains, having deep HOMO energy levels (∼−5.4 eV). The synthesis of the polymers is achieved in a few synthetic and purification steps at reduced cost. The theoretical calculations uncover that the dielectric environmental variations are responsible for the observed band gap lowering in OEG-based polymers compared to their alkylated counterparts. Notably, the aqueous-processed all-polymer solar cells (aq-APSCs) based on P(Qx8O-T) and poly[( N, N ′-bis(3-(2-(2-(2-methoxyethoxy)-ethoxy)ethoxy)-2-((2-(2-(2-methoxyethoxy)ethoxy)ethoxy)-methyl)propyl)naphthalene-1,4,5,8-bis(dicarboximide)-2,6-diyl)- alt -(2,5-thiophene)] ( P(NDIDEG-T) ) active layer exhibit a PCE of 2.27% and high open-circuit voltage ( V OC ) approaching 0.8 V, which are among the highest values for aq-APSCs reported to date. This study provides important clues for the design of low-cost, aqueous-processable polymer donors and the fabrication of aqueous-processable OSCs with high V OC .
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Affiliations
Department of Chemistry and Chemical Engineering, Chalmers University of Technology, SE-412 96 Göteborg, Sweden
Department of Chemistry, Addis Ababa University, P.O. Box 33658, 1000 Addis Ababa, Ethiopia
Department of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science and Technology (KAIST), 34141 Daejeon, Republic of Korea
Energy Materials Research Center, Korea Research Institute of Chemical Technology (KRICT), 34114 Daejeon, Republic of Korea
Department of Engineering and Physics, Karlstad University, 65188 Karlstad, Sweden
Department of Chemistry, Korea University, 02841 Seoul, Republic of Korea
Materials Theory Division, Department of Physics and Astronomy, Uppsala University, 75120 Uppsala, Sweden
Funding
Svenska Forskningsr?det Formas · Vetenskapsr?det · Uppsala Universitet · National Research Foundation of Korea · Knut och Alice Wallenbergs Stiftelse · Swedish Foundation for International Cooperation in Research and Higher Education