{"title":"2-乙基己基-4,6-二溴-3-氰-3-噻吩[3,4-b]成为低HOMO能级聚合物供体","authors":"Lei Wang, Yude Liu, Lihua Cao, Xiaohong Zhao, Haigang Li, Zhongyi Yuan","doi":"10.1002/macp.202400317","DOIUrl":null,"url":null,"abstract":"<p>The new halogen-free donor polymer PCN6 is constructed using 2-ethylhexyl-4,6-dibromo-3-cyano-thieno[3,4-b]thiophene as acceptor (A) block, and is compared in detail with the commercially available PTB7-Th. It is found that PCN6 has a wider film absorption (300–700 nm) and lower highest occupied molecular orbital (HOMO) energy levels (−5.52 eV) than PTB7-Th (−5.34 eV), suggesting a great advantage of the monocyano-functionalized modification strategy in terms of molecular absorption and energy level tuning. The performance difference between PCN6:Y6- and PTB7-Th:Y6-based organic solar cells (OSCs) is compared by a series of studies including light intensity dependence, carrier mobility, AFM, TEM, and GIWAXS. The results show that PCN6:Y6-based OSCs have stronger crystallinity, better charge transport, higher and more balanced carrier mobility, and less exciton complex loss. Therefore, the power conversion efficiency (PCE) of PCN6:Y6-based OSCs reaches 11.34%, while the PCE of PTB7-Th:Y6-based OSCs is only 9.02%. These results suggest that 2-ethylhexyl-4,6-dibromo-3-cyano-thieno[3,4-b]thiophene is an excellent A block for the construction of halogen-free donor polymers with low HOMO energy levels, and also demonstrate that the introduction of cyano in the conjugated backbone of polymers is a good strategy to achieve high-performance OSCs.</p>","PeriodicalId":18054,"journal":{"name":"Macromolecular Chemistry and Physics","volume":"226 1","pages":""},"PeriodicalIF":2.5000,"publicationDate":"2024-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"2-Ethylhexyl-4,6-Dibromo-3-Cyano-3-Thieno[3,4-b]Thiophene Enables Low HOMO Energy Level Polymer Donor\",\"authors\":\"Lei Wang, Yude Liu, Lihua Cao, Xiaohong Zhao, Haigang Li, Zhongyi Yuan\",\"doi\":\"10.1002/macp.202400317\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The new halogen-free donor polymer PCN6 is constructed using 2-ethylhexyl-4,6-dibromo-3-cyano-thieno[3,4-b]thiophene as acceptor (A) block, and is compared in detail with the commercially available PTB7-Th. It is found that PCN6 has a wider film absorption (300–700 nm) and lower highest occupied molecular orbital (HOMO) energy levels (−5.52 eV) than PTB7-Th (−5.34 eV), suggesting a great advantage of the monocyano-functionalized modification strategy in terms of molecular absorption and energy level tuning. The performance difference between PCN6:Y6- and PTB7-Th:Y6-based organic solar cells (OSCs) is compared by a series of studies including light intensity dependence, carrier mobility, AFM, TEM, and GIWAXS. The results show that PCN6:Y6-based OSCs have stronger crystallinity, better charge transport, higher and more balanced carrier mobility, and less exciton complex loss. Therefore, the power conversion efficiency (PCE) of PCN6:Y6-based OSCs reaches 11.34%, while the PCE of PTB7-Th:Y6-based OSCs is only 9.02%. These results suggest that 2-ethylhexyl-4,6-dibromo-3-cyano-thieno[3,4-b]thiophene is an excellent A block for the construction of halogen-free donor polymers with low HOMO energy levels, and also demonstrate that the introduction of cyano in the conjugated backbone of polymers is a good strategy to achieve high-performance OSCs.</p>\",\"PeriodicalId\":18054,\"journal\":{\"name\":\"Macromolecular Chemistry and Physics\",\"volume\":\"226 1\",\"pages\":\"\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2024-11-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Macromolecular Chemistry and Physics\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/macp.202400317\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"POLYMER SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Macromolecular Chemistry and Physics","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/macp.202400317","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
2-Ethylhexyl-4,6-Dibromo-3-Cyano-3-Thieno[3,4-b]Thiophene Enables Low HOMO Energy Level Polymer Donor
The new halogen-free donor polymer PCN6 is constructed using 2-ethylhexyl-4,6-dibromo-3-cyano-thieno[3,4-b]thiophene as acceptor (A) block, and is compared in detail with the commercially available PTB7-Th. It is found that PCN6 has a wider film absorption (300–700 nm) and lower highest occupied molecular orbital (HOMO) energy levels (−5.52 eV) than PTB7-Th (−5.34 eV), suggesting a great advantage of the monocyano-functionalized modification strategy in terms of molecular absorption and energy level tuning. The performance difference between PCN6:Y6- and PTB7-Th:Y6-based organic solar cells (OSCs) is compared by a series of studies including light intensity dependence, carrier mobility, AFM, TEM, and GIWAXS. The results show that PCN6:Y6-based OSCs have stronger crystallinity, better charge transport, higher and more balanced carrier mobility, and less exciton complex loss. Therefore, the power conversion efficiency (PCE) of PCN6:Y6-based OSCs reaches 11.34%, while the PCE of PTB7-Th:Y6-based OSCs is only 9.02%. These results suggest that 2-ethylhexyl-4,6-dibromo-3-cyano-thieno[3,4-b]thiophene is an excellent A block for the construction of halogen-free donor polymers with low HOMO energy levels, and also demonstrate that the introduction of cyano in the conjugated backbone of polymers is a good strategy to achieve high-performance OSCs.
期刊介绍:
Macromolecular Chemistry and Physics publishes in all areas of polymer science - from chemistry, physical chemistry, and physics of polymers to polymers in materials science. Beside an attractive mixture of high-quality Full Papers, Trends, and Highlights, the journal offers a unique article type dedicated to young scientists – Talent.