KMS Qingdao Institute of Biomass Energy and Bioprocess Technology ,CAS
| Modifying the morphology via employing rigid phenyl side chains achieves efficient nonfullerene polymer solar cells | |
Zhong, Yaqian1,2; Liu, Deyu2,3; Zhang, Kaili1,2; Li, Yonghai2; Sun, Mingliang1,4; Yu, Liangmin4; Li, Feng5; Liu, Huizhou2 ; Yang, Renqiang2
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| 2018-12-15 | |
| Source Publication | JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
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| ISSN | 0887-624X |
| Volume | 56Issue:24Pages:2762-2770 |
| Abstract | As a promising electron-deficient (acceptor) unit, fluorinated benzotriazole (TAZ) was used widely to construct wide bandgap polymers for nonfullerene polymer solar cells (NF-PSCs). However, due to the S horizontal ellipsis F noncovalent interaction, the unit show good planarity and strong aggregation, which was not beneficial for the blend with the elongated nonfullerene acceptors. Here, we tried to choose new donor polymers to match with TAZ unit, which was expected to destroy the interchain aggregation of polymer and form favorable morphology of blends. Two new wide-bandgap polymers PBDTsPhPh-T1 and PBDTsThPh-T1 based on the unsymmetrical benzodithiophene (BDT) units with a benzene ring as lever arms were synthesized. As a result, these two polymers blend well with nonfullerene acceptor (ITIC). And then, PBDTsPhPh-T1 and PBDTsThPh-T1-based devices exhibit the decent photovoltaic properties with high power conversion efficiencies of 8.85 and 9.34%, respectively. The work demonstrates that the unsymmetrical BDT units could be outstanding for building donor materials toward high-performance NF-PSCs. (c) 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2018, 56, 2762-2770 |
| Keyword | fluorinated benzotriazole lever arms nonfullerene acceptor polymer solar cells unsymmetrical benzodithiophene |
| DOI | 10.1002/pola.29264 |
| WOS Keyword | PERFORMANCE ; ACCEPTOR ; ALKYLTHIO ; DONOR |
| Language | 英语 |
| Funding Project | National Natural Science Foundation of China[51573205] ; National Natural Science Foundation of China[51773220] ; Natural Science Foundation of Shandong Province[ZR2018MEM023] ; Fundamental Research Funds for the Central Universities[201822002] ; Taishan Scholars Climbing Program of Shandong[tspd20150210] |
| WOS Research Area | Polymer Science |
| Funding Organization | National Natural Science Foundation of China ; Natural Science Foundation of Shandong Province ; Fundamental Research Funds for the Central Universities ; Taishan Scholars Climbing Program of Shandong |
| WOS Subject | Polymer Science |
| WOS ID | WOS:000450460600007 |
| Publisher | WILEY |
| Citation statistics | |
| Document Type | 期刊论文 |
| Identifier | http://ir.qibebt.ac.cn/handle/337004/11035 |
| Collection | 中国科学院青岛生物能源与过程研究所 |
| Corresponding Author | Sun, Mingliang; Liu, Huizhou; Yang, Renqiang |
| Affiliation | 1.Ocean Univ China, Sch Mat Sci & Engn, Qingdao 266100, Peoples R China 2.Chinese Acad Sci, Qingdao Inst Bioenergy & Bioproc Technol, CAS Key Lab Biobased Mat, Qingdao 266101, Peoples R China 3.Univ Chinese Acad Sci, Beijing 100049, Peoples R China 4.Qingdao Natl Lab Marine Sci & Technol, Qingdao 266100, Peoples R China 5.Qingdao Univ Sci & Technol, Sch Polymer Sci & Engn, Minist Educ Shandong Prov, Key Lab Rubber Plast, Qingdao 266042, Peoples R China |
| Recommended Citation GB/T 7714 | Zhong, Yaqian,Liu, Deyu,Zhang, Kaili,et al. Modifying the morphology via employing rigid phenyl side chains achieves efficient nonfullerene polymer solar cells[J]. JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY,2018,56(24):2762-2770. |
| APA | Zhong, Yaqian.,Liu, Deyu.,Zhang, Kaili.,Li, Yonghai.,Sun, Mingliang.,...&Yang, Renqiang.(2018).Modifying the morphology via employing rigid phenyl side chains achieves efficient nonfullerene polymer solar cells.JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY,56(24),2762-2770. |
| MLA | Zhong, Yaqian,et al."Modifying the morphology via employing rigid phenyl side chains achieves efficient nonfullerene polymer solar cells".JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY 56.24(2018):2762-2770. |
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