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Chlorination of Low-Band-Gap Polymers: Toward High-Performance Polymer Solar Cells
Halogenation is an effective way to tune the energy levels of organic semiconducting materials. To date, fluorination of organic semiconducting materials to fabricate polymer solar cells (PSCs) has been used far more than chlorination; however, fluorine exchange reactions suffer from low yields and...
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Published in: | Chemistry of materials 2017-04, Vol.29 (7), p.2819-2830 |
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container_title | Chemistry of materials |
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creator | Mo, Daize Wang, Huan Chen, Hui Qu, Shiwei Chao, Pengjie Yang, Zhen Tian, Leilei Su, Yu-An Gao, Yu Yang, Bing Chen, Wei He, Feng |
description | Halogenation is an effective way to tune the energy levels of organic semiconducting materials. To date, fluorination of organic semiconducting materials to fabricate polymer solar cells (PSCs) has been used far more than chlorination; however, fluorine exchange reactions suffer from low yields and the resulting fluorinated polymer always comes with a higher price, which will greatly hinder their commercial applications. Herein, we designed and synthesized a series of chlorinated donor–acceptor (D-A) type polymers, in which benzo[1,2-b:4,5-b]dithiophene and chlorinated benzothiadiazole units are connected by thiophene π-bridges with an asymmetric alkyl chain. These chlorinated polymers showed deep highest occupied molecular orbital (HOMO) energy levels, which promoted the efficiency of their corresponding PSCs by increasing the device open circuit voltage. The asymmetric alkyl chain on the thiophene moieties gave the final polymer sufficient solubility for solution processing and strong π–π stacking in films allowed for high mobility. Although the introduction of a large Cl atom increased the torsion angle of the polymer backbone, the chlorinated polymers maintained a favorable backbone orientation in blend films for efficient PSC application. These factors contributed to respectable device performances from thick-film devices, which showed PCEs as high as 9.11% for a 250-nm-thick active layer. These results demonstrate that chlorination is a promising method to fine-tune the energy levels of conjugated polymers, and chlorinated benzothiadiazole may be a versatile building block in materials for efficient solar energy conversion. |
doi_str_mv | 10.1021/acs.chemmater.6b04828 |
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To date, fluorination of organic semiconducting materials to fabricate polymer solar cells (PSCs) has been used far more than chlorination; however, fluorine exchange reactions suffer from low yields and the resulting fluorinated polymer always comes with a higher price, which will greatly hinder their commercial applications. Herein, we designed and synthesized a series of chlorinated donor–acceptor (D-A) type polymers, in which benzo[1,2-b:4,5-b]dithiophene and chlorinated benzothiadiazole units are connected by thiophene π-bridges with an asymmetric alkyl chain. These chlorinated polymers showed deep highest occupied molecular orbital (HOMO) energy levels, which promoted the efficiency of their corresponding PSCs by increasing the device open circuit voltage. The asymmetric alkyl chain on the thiophene moieties gave the final polymer sufficient solubility for solution processing and strong π–π stacking in films allowed for high mobility. Although the introduction of a large Cl atom increased the torsion angle of the polymer backbone, the chlorinated polymers maintained a favorable backbone orientation in blend films for efficient PSC application. These factors contributed to respectable device performances from thick-film devices, which showed PCEs as high as 9.11% for a 250-nm-thick active layer. 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The asymmetric alkyl chain on the thiophene moieties gave the final polymer sufficient solubility for solution processing and strong π–π stacking in films allowed for high mobility. Although the introduction of a large Cl atom increased the torsion angle of the polymer backbone, the chlorinated polymers maintained a favorable backbone orientation in blend films for efficient PSC application. These factors contributed to respectable device performances from thick-film devices, which showed PCEs as high as 9.11% for a 250-nm-thick active layer. 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Mater</addtitle><date>2017-04-11</date><risdate>2017</risdate><volume>29</volume><issue>7</issue><spage>2819</spage><epage>2830</epage><pages>2819-2830</pages><issn>0897-4756</issn><eissn>1520-5002</eissn><abstract>Halogenation is an effective way to tune the energy levels of organic semiconducting materials. To date, fluorination of organic semiconducting materials to fabricate polymer solar cells (PSCs) has been used far more than chlorination; however, fluorine exchange reactions suffer from low yields and the resulting fluorinated polymer always comes with a higher price, which will greatly hinder their commercial applications. Herein, we designed and synthesized a series of chlorinated donor–acceptor (D-A) type polymers, in which benzo[1,2-b:4,5-b]dithiophene and chlorinated benzothiadiazole units are connected by thiophene π-bridges with an asymmetric alkyl chain. 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title | Chlorination of Low-Band-Gap Polymers: Toward High-Performance Polymer Solar Cells |
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