Search references:
| 1. | Zhao, Heng; Naveed, Hafiz Bilal; Lin, Baojun; Zhou, Xiaobo; Yuan, Jian; Zhou, Ke; Wu, Hongbo; Guo, Renjun; Scheel, Manuel A; Chumakov, Andrei; Roth, Stephan V; Tang, Zheng; Müller-Buschbaum, Peter; Ma, Wei: Hot Hydrocarbon-Solvent Slot-Die Coating Enables High-Efficiency Organic Solar Cells with Temperature-Dependent Aggregation Behavior. In: Advanced Materials, 32 (39), pp. 2002302, 2020. (Type: Journal Article | Abstract | Links | BibTeX) @article{Zhao2020, title = {Hot Hydrocarbon-Solvent Slot-Die Coating Enables High-Efficiency Organic Solar Cells with Temperature-Dependent Aggregation Behavior}, author = {Heng Zhao and Hafiz Bilal Naveed and Baojun Lin and Xiaobo Zhou and Jian Yuan and Ke Zhou and Hongbo Wu and Renjun Guo and Manuel A Scheel and Andrei Chumakov and Stephan V Roth and Zheng Tang and Peter Müller-Buschbaum and Wei Ma}, url = {https://onlinelibrary.wiley.com/doi/abs/10.1002/adma.202002302}, doi = {https://doi.org/10.1002/adma.202002302}, year = {2020}, date = {2020-01-01}, journal = {Advanced Materials}, volume = {32}, number = {39}, pages = {2002302}, abstract = {Abstract Organic solar cells (OSCs) have made rapid progress in terms of their development as a sustainable energy source. However, record-breaking devices have not shown compatibility with large-scale production via solution processing in particular due to the use of halogenated environment-threatening solvents. Here, slot-die fabrication with processing involving hydrocarbon-based solvents is used to realize highly efficient and environmentally friendly OSCs. Highly compatible slot-die coating with roll-to-roll processing using halogenated (chlorobenzene (CB)) and hydrocarbon solvents (1,2,4-trimethylbenzene (TMB) and ortho-xylene (o-XY)) is used to fabricate photoactive films. Controlled solution and substrate temperatures enable similar aggregation states in the solution and similar kinetics processes during film formation. The optimized blend film nanostructures for different solvents in the highly efficient PM6:Y6 blend is adopted to show a similar morphology, which results in device efficiencies of 15.2%, 15.4%, and 15.6% for CB, TMB, and o-XY solvents. This approach is successfully extended to other donor–acceptor combinations to demonstrate the excellent universality of this method. The results combine a method to optimize the aggregation state and film formation kinetics with the fabrication of OSCs with environmentally friendly solvents by slot-die coating, which is a critical finding for the future development of OSCs in terms of their scalable production and high-performance.}, keywords = {}, pubstate = {published}, tppubtype = {article} } Abstract Organic solar cells (OSCs) have made rapid progress in terms of their development as a sustainable energy source. However, record-breaking devices have not shown compatibility with large-scale production via solution processing in particular due to the use of halogenated environment-threatening solvents. Here, slot-die fabrication with processing involving hydrocarbon-based solvents is used to realize highly efficient and environmentally friendly OSCs. Highly compatible slot-die coating with roll-to-roll processing using halogenated (chlorobenzene (CB)) and hydrocarbon solvents (1,2,4-trimethylbenzene (TMB) and ortho-xylene (o-XY)) is used to fabricate photoactive films. Controlled solution and substrate temperatures enable similar aggregation states in the solution and similar kinetics processes during film formation. The optimized blend film nanostructures for different solvents in the highly efficient PM6:Y6 blend is adopted to show a similar morphology, which results in device efficiencies of 15.2%, 15.4%, and 15.6% for CB, TMB, and o-XY solvents. This approach is successfully extended to other donor–acceptor combinations to demonstrate the excellent universality of this method. The results combine a method to optimize the aggregation state and film formation kinetics with the fabrication of OSCs with environmentally friendly solvents by slot-die coating, which is a critical finding for the future development of OSCs in terms of their scalable production and high-performance. |
| 2. | Wienhold, Kerstin S; Chen, Wei; Yin, Shanshan; Guo, Renjun; Schwartzkopf, Matthias; Roth, Stephan V; Müller-Buschbaum, Peter: Following in Operando the Structure Evolution-Induced Degradation in Printed Organic Solar Cells with Nonfullerene Small Molecule Acceptor. In: Solar RRL, 4 (9), pp. 2000251, 2020. (Type: Journal Article | Abstract | Links | BibTeX) @article{Wienhold2020a, title = {Following in Operando the Structure Evolution-Induced Degradation in Printed Organic Solar Cells with Nonfullerene Small Molecule Acceptor}, author = {Kerstin S Wienhold and Wei Chen and Shanshan Yin and Renjun Guo and Matthias Schwartzkopf and Stephan V Roth and Peter Müller-Buschbaum}, url = {https://onlinelibrary.wiley.com/doi/abs/10.1002/solr.202000251}, doi = {https://doi.org/10.1002/solr.202000251}, year = {2020}, date = {2020-01-01}, journal = {Solar RRL}, volume = {4}, number = {9}, pages = {2000251}, abstract = {Understanding the degradation mechanisms of printed bulk-heterojunction (BHJ) organic solar cells during operation is essential to achieve long-term stability and realize real-world applications of organic photovoltaics. Herein, the degradation of printed organic solar cells based on the conjugated benzodithiophene polymer PBDB-T-SF and the nonfullerene small molecule acceptor IT-4F with 0.25 vol% 1,8-diiodooctane (DIO) solvent additive is studied in operando for two different donor:acceptor ratios. The inner nano-morphology is analyzed with grazing incidence small angle X-ray scattering (GISAXS), and current–voltage (I–V) characteristics are probed simultaneously. Irrespective of the mixing ratio, degradation occurs by the same degradation mechanism. A decrease in the short-circuit current density (JSC) is identified to be the determining factor for the decline of the power conversion efficiency. The decrease in JSC is induced by a reduction of the relative interface area between the conjugated polymer and the small molecule acceptor in the BHJ structure, resembling the morphological degradation of the active layer.}, keywords = {}, pubstate = {published}, tppubtype = {article} } Understanding the degradation mechanisms of printed bulk-heterojunction (BHJ) organic solar cells during operation is essential to achieve long-term stability and realize real-world applications of organic photovoltaics. Herein, the degradation of printed organic solar cells based on the conjugated benzodithiophene polymer PBDB-T-SF and the nonfullerene small molecule acceptor IT-4F with 0.25 vol% 1,8-diiodooctane (DIO) solvent additive is studied in operando for two different donor:acceptor ratios. The inner nano-morphology is analyzed with grazing incidence small angle X-ray scattering (GISAXS), and current–voltage (I–V) characteristics are probed simultaneously. Irrespective of the mixing ratio, degradation occurs by the same degradation mechanism. A decrease in the short-circuit current density (JSC) is identified to be the determining factor for the decline of the power conversion efficiency. The decrease in JSC is induced by a reduction of the relative interface area between the conjugated polymer and the small molecule acceptor in the BHJ structure, resembling the morphological degradation of the active layer. |
References (last update: Dec 16, 2019):
2020 |
Zhao, Heng; Naveed, Hafiz Bilal; Lin, Baojun; Zhou, Xiaobo; Yuan, Jian; Zhou, Ke; Wu, Hongbo; Guo, Renjun; Scheel, Manuel A; Chumakov, Andrei; Roth, Stephan V; Tang, Zheng; Müller-Buschbaum, Peter; Ma, Wei Hot Hydrocarbon-Solvent Slot-Die Coating Enables High-Efficiency Organic Solar Cells with Temperature-Dependent Aggregation Behavior Journal Article Advanced Materials, 32 (39), pp. 2002302, 2020. Abstract | Links | BibTeX | Tags: hot slot-die coating, hydrocarbon solvents, organic solar cells, temperature-dependent aggregation @article{Zhao2020, title = {Hot Hydrocarbon-Solvent Slot-Die Coating Enables High-Efficiency Organic Solar Cells with Temperature-Dependent Aggregation Behavior}, author = {Heng Zhao and Hafiz Bilal Naveed and Baojun Lin and Xiaobo Zhou and Jian Yuan and Ke Zhou and Hongbo Wu and Renjun Guo and Manuel A Scheel and Andrei Chumakov and Stephan V Roth and Zheng Tang and Peter Müller-Buschbaum and Wei Ma}, url = {https://onlinelibrary.wiley.com/doi/abs/10.1002/adma.202002302}, doi = {https://doi.org/10.1002/adma.202002302}, year = {2020}, date = {2020-01-01}, journal = {Advanced Materials}, volume = {32}, number = {39}, pages = {2002302}, abstract = {Abstract Organic solar cells (OSCs) have made rapid progress in terms of their development as a sustainable energy source. However, record-breaking devices have not shown compatibility with large-scale production via solution processing in particular due to the use of halogenated environment-threatening solvents. Here, slot-die fabrication with processing involving hydrocarbon-based solvents is used to realize highly efficient and environmentally friendly OSCs. Highly compatible slot-die coating with roll-to-roll processing using halogenated (chlorobenzene (CB)) and hydrocarbon solvents (1,2,4-trimethylbenzene (TMB) and ortho-xylene (o-XY)) is used to fabricate photoactive films. Controlled solution and substrate temperatures enable similar aggregation states in the solution and similar kinetics processes during film formation. The optimized blend film nanostructures for different solvents in the highly efficient PM6:Y6 blend is adopted to show a similar morphology, which results in device efficiencies of 15.2%, 15.4%, and 15.6% for CB, TMB, and o-XY solvents. This approach is successfully extended to other donor–acceptor combinations to demonstrate the excellent universality of this method. The results combine a method to optimize the aggregation state and film formation kinetics with the fabrication of OSCs with environmentally friendly solvents by slot-die coating, which is a critical finding for the future development of OSCs in terms of their scalable production and high-performance.}, keywords = {hot slot-die coating, hydrocarbon solvents, organic solar cells, temperature-dependent aggregation}, pubstate = {published}, tppubtype = {article} } Abstract Organic solar cells (OSCs) have made rapid progress in terms of their development as a sustainable energy source. However, record-breaking devices have not shown compatibility with large-scale production via solution processing in particular due to the use of halogenated environment-threatening solvents. Here, slot-die fabrication with processing involving hydrocarbon-based solvents is used to realize highly efficient and environmentally friendly OSCs. Highly compatible slot-die coating with roll-to-roll processing using halogenated (chlorobenzene (CB)) and hydrocarbon solvents (1,2,4-trimethylbenzene (TMB) and ortho-xylene (o-XY)) is used to fabricate photoactive films. Controlled solution and substrate temperatures enable similar aggregation states in the solution and similar kinetics processes during film formation. The optimized blend film nanostructures for different solvents in the highly efficient PM6:Y6 blend is adopted to show a similar morphology, which results in device efficiencies of 15.2%, 15.4%, and 15.6% for CB, TMB, and o-XY solvents. This approach is successfully extended to other donor–acceptor combinations to demonstrate the excellent universality of this method. The results combine a method to optimize the aggregation state and film formation kinetics with the fabrication of OSCs with environmentally friendly solvents by slot-die coating, which is a critical finding for the future development of OSCs in terms of their scalable production and high-performance. |
Wienhold, Kerstin S; Chen, Wei; Yin, Shanshan; Guo, Renjun; Schwartzkopf, Matthias; Roth, Stephan V; Müller-Buschbaum, Peter Following in Operando the Structure Evolution-Induced Degradation in Printed Organic Solar Cells with Nonfullerene Small Molecule Acceptor Journal Article Solar RRL, 4 (9), pp. 2000251, 2020. Abstract | Links | BibTeX | Tags: degradation mechanisms, meniscus-guided slot-die coatings, organic solar cells, short-circuit currents @article{Wienhold2020a, title = {Following in Operando the Structure Evolution-Induced Degradation in Printed Organic Solar Cells with Nonfullerene Small Molecule Acceptor}, author = {Kerstin S Wienhold and Wei Chen and Shanshan Yin and Renjun Guo and Matthias Schwartzkopf and Stephan V Roth and Peter Müller-Buschbaum}, url = {https://onlinelibrary.wiley.com/doi/abs/10.1002/solr.202000251}, doi = {https://doi.org/10.1002/solr.202000251}, year = {2020}, date = {2020-01-01}, journal = {Solar RRL}, volume = {4}, number = {9}, pages = {2000251}, abstract = {Understanding the degradation mechanisms of printed bulk-heterojunction (BHJ) organic solar cells during operation is essential to achieve long-term stability and realize real-world applications of organic photovoltaics. Herein, the degradation of printed organic solar cells based on the conjugated benzodithiophene polymer PBDB-T-SF and the nonfullerene small molecule acceptor IT-4F with 0.25 vol% 1,8-diiodooctane (DIO) solvent additive is studied in operando for two different donor:acceptor ratios. The inner nano-morphology is analyzed with grazing incidence small angle X-ray scattering (GISAXS), and current–voltage (I–V) characteristics are probed simultaneously. Irrespective of the mixing ratio, degradation occurs by the same degradation mechanism. A decrease in the short-circuit current density (JSC) is identified to be the determining factor for the decline of the power conversion efficiency. The decrease in JSC is induced by a reduction of the relative interface area between the conjugated polymer and the small molecule acceptor in the BHJ structure, resembling the morphological degradation of the active layer.}, keywords = {degradation mechanisms, meniscus-guided slot-die coatings, organic solar cells, short-circuit currents}, pubstate = {published}, tppubtype = {article} } Understanding the degradation mechanisms of printed bulk-heterojunction (BHJ) organic solar cells during operation is essential to achieve long-term stability and realize real-world applications of organic photovoltaics. Herein, the degradation of printed organic solar cells based on the conjugated benzodithiophene polymer PBDB-T-SF and the nonfullerene small molecule acceptor IT-4F with 0.25 vol% 1,8-diiodooctane (DIO) solvent additive is studied in operando for two different donor:acceptor ratios. The inner nano-morphology is analyzed with grazing incidence small angle X-ray scattering (GISAXS), and current–voltage (I–V) characteristics are probed simultaneously. Irrespective of the mixing ratio, degradation occurs by the same degradation mechanism. A decrease in the short-circuit current density (JSC) is identified to be the determining factor for the decline of the power conversion efficiency. The decrease in JSC is induced by a reduction of the relative interface area between the conjugated polymer and the small molecule acceptor in the BHJ structure, resembling the morphological degradation of the active layer. |