{"title":"通过使用部分氟化侧链增强 M 系列受体的骨架组织和光伏性能","authors":"","doi":"10.1016/j.chempr.2024.06.005","DOIUrl":null,"url":null,"abstract":"<div><div><span><span>Side-chain fluorination<span> of nonfullerene acceptors (NFAs) has been rarely reported to enhance their photovoltaic performance, although it may improve their backbone organization and </span></span>carrier mobilities. Here, we design new partially fluorinated side chains and incorporate them into M-series NFAs, which are featured with a ladder-type heteroheptacene-cored skeleton without </span><em>sp</em><sup>3</sup><span><span>-hybridized carbons. Compared with the traditional M-series acceptor with non-fluorinated side chains (MC7F0), the NFA with partially fluorinated side chains (MC7F3) shows down-shifted energy levels, reduced miscibility, and more importantly, improved backbone organization, thereby leading to the formation of a 3D network packing structure with enhanced carrier transport. Consequently, the MC7F3-based device exhibits a power conversion efficiency of 17.61% and an excellent fill factor of 79.48%, both of which are among the best values for all A-D-A-type NFAs reported so far. The results highlight that side-chain fluorination can efficiently enhance π-conjugated backbone organization, improve intermolecular interaction, increase </span>electron mobilities, and boost photovoltaic performance of NFAs.</span></div></div>","PeriodicalId":268,"journal":{"name":"Chem","volume":"10 10","pages":"Pages 3131-3147"},"PeriodicalIF":19.1000,"publicationDate":"2024-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Enhancing backbone organization and photovoltaic performance of M-series acceptors by using partially fluorinated side chains\",\"authors\":\"\",\"doi\":\"10.1016/j.chempr.2024.06.005\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div><span><span>Side-chain fluorination<span> of nonfullerene acceptors (NFAs) has been rarely reported to enhance their photovoltaic performance, although it may improve their backbone organization and </span></span>carrier mobilities. Here, we design new partially fluorinated side chains and incorporate them into M-series NFAs, which are featured with a ladder-type heteroheptacene-cored skeleton without </span><em>sp</em><sup>3</sup><span><span>-hybridized carbons. Compared with the traditional M-series acceptor with non-fluorinated side chains (MC7F0), the NFA with partially fluorinated side chains (MC7F3) shows down-shifted energy levels, reduced miscibility, and more importantly, improved backbone organization, thereby leading to the formation of a 3D network packing structure with enhanced carrier transport. Consequently, the MC7F3-based device exhibits a power conversion efficiency of 17.61% and an excellent fill factor of 79.48%, both of which are among the best values for all A-D-A-type NFAs reported so far. The results highlight that side-chain fluorination can efficiently enhance π-conjugated backbone organization, improve intermolecular interaction, increase </span>electron mobilities, and boost photovoltaic performance of NFAs.</span></div></div>\",\"PeriodicalId\":268,\"journal\":{\"name\":\"Chem\",\"volume\":\"10 10\",\"pages\":\"Pages 3131-3147\"},\"PeriodicalIF\":19.1000,\"publicationDate\":\"2024-10-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chem\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2451929424002523\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chem","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2451929424002523","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
摘要
非富勒烯受体(NFAs)的侧链氟化可改善其骨架组织和载流子迁移率,但很少有报道称氟化可提高其光伏性能。在这里,我们设计了新的部分氟化侧链,并将其加入到 M 系列非富勒烯受体中,这种受体具有梯形杂七烯芯骨架,没有 sp3 杂化碳。与传统的带有非氟化侧链的 M 系列受体(MC7F0)相比,带有部分氟化侧链的 NFA(MC7F3)能级下移,混溶性降低,更重要的是骨架组织得到改善,从而形成了三维网络堆积结构,载流子传输能力增强。因此,基于 MC7F3 的器件显示出 17.61% 的功率转换效率和 79.48% 的出色填充因子,这两项指标都是迄今所报道的所有 A-D-A 型 NFA 的最佳值之一。研究结果表明,侧链氟化可有效增强π-共轭骨架组织,改善分子间相互作用,提高电子迁移率,从而提高 NFA 的光伏性能。
Enhancing backbone organization and photovoltaic performance of M-series acceptors by using partially fluorinated side chains
Side-chain fluorination of nonfullerene acceptors (NFAs) has been rarely reported to enhance their photovoltaic performance, although it may improve their backbone organization and carrier mobilities. Here, we design new partially fluorinated side chains and incorporate them into M-series NFAs, which are featured with a ladder-type heteroheptacene-cored skeleton without sp3-hybridized carbons. Compared with the traditional M-series acceptor with non-fluorinated side chains (MC7F0), the NFA with partially fluorinated side chains (MC7F3) shows down-shifted energy levels, reduced miscibility, and more importantly, improved backbone organization, thereby leading to the formation of a 3D network packing structure with enhanced carrier transport. Consequently, the MC7F3-based device exhibits a power conversion efficiency of 17.61% and an excellent fill factor of 79.48%, both of which are among the best values for all A-D-A-type NFAs reported so far. The results highlight that side-chain fluorination can efficiently enhance π-conjugated backbone organization, improve intermolecular interaction, increase electron mobilities, and boost photovoltaic performance of NFAs.
期刊介绍:
Chem, affiliated with Cell as its sister journal, serves as a platform for groundbreaking research and illustrates how fundamental inquiries in chemistry and its related fields can contribute to addressing future global challenges. It was established in 2016, and is currently edited by Robert Eagling.