New wide band gap π-conjugated copolymers based on anthra[1,2-b: 4,3-b': 6,7-c''] trithiophene-8,12-dione for high performance non-fullerene polymer solar cells with an efficiency of 15.07 %

IF 4.5 2区 化学 Q2 POLYMER SCIENCE Polymer Pub Date : 2022-06-03 DOI:10.1016/j.polymer.2022.124892
Mukhamed L. Keshtov , Igor O. Konstantinov , Alexei R. Khokhlov , Sergei A. Kuklin , Vladimir G. Alekseev , Ilya E. Ostapov , Yingping Zou , Rahul Singhal , Hemraj Dahiya , Ganesh D. Sharma
{"title":"New wide band gap π-conjugated copolymers based on anthra[1,2-b: 4,3-b': 6,7-c''] trithiophene-8,12-dione for high performance non-fullerene polymer solar cells with an efficiency of 15.07 %","authors":"Mukhamed L. Keshtov ,&nbsp;Igor O. Konstantinov ,&nbsp;Alexei R. Khokhlov ,&nbsp;Sergei A. Kuklin ,&nbsp;Vladimir G. Alekseev ,&nbsp;Ilya E. Ostapov ,&nbsp;Yingping Zou ,&nbsp;Rahul Singhal ,&nbsp;Hemraj Dahiya ,&nbsp;Ganesh D. Sharma","doi":"10.1016/j.polymer.2022.124892","DOIUrl":null,"url":null,"abstract":"<div><p><span><span>Developing efficient wide-bandgap copolymer donor materials to match with narrow bandgap non-fullerene acceptors is continuously ongoing for </span>polymer solar cells. Herein, two new D-A copolymers are designed and synthesized by embedding the same anthra[1,2-b:4,3-b':6,7-c\"] trithiophene-8,12-dione (A3T) acceptor unit and different donor units, i.e., BDTTZ (</span><strong>P126</strong>) and BDTTh (<strong>P127</strong><span>). These copolymers showed broad absorption from 350 to 680 nm and deeper HOMO energy level. We have used these two copolymers as donors and a narrow bandgap non-fullerene acceptor Y6 to prepare bulk heterojunction polymer solar cells (PSCs). After the optimization, </span><strong>P126</strong>:Y6 and <strong>P127</strong>:Y6 attained overall power conversion efficiency of 15.07% and 12.27%, respectively. The higher PCE for the <strong>P126</strong> than <strong>P127</strong><span> is associated with the more efficient photon harvesting and photogenerated excitons, balanced charge transport, and low energy loss. Our results may help to design new polymers with a deeper highest occupied molecular orbital level that will be well-matched with non-fullerene acceptors.</span></p></div>","PeriodicalId":405,"journal":{"name":"Polymer","volume":"251 ","pages":"Article 124892"},"PeriodicalIF":4.5000,"publicationDate":"2022-06-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polymer","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0032386122003809","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 3

Abstract

Developing efficient wide-bandgap copolymer donor materials to match with narrow bandgap non-fullerene acceptors is continuously ongoing for polymer solar cells. Herein, two new D-A copolymers are designed and synthesized by embedding the same anthra[1,2-b:4,3-b':6,7-c"] trithiophene-8,12-dione (A3T) acceptor unit and different donor units, i.e., BDTTZ (P126) and BDTTh (P127). These copolymers showed broad absorption from 350 to 680 nm and deeper HOMO energy level. We have used these two copolymers as donors and a narrow bandgap non-fullerene acceptor Y6 to prepare bulk heterojunction polymer solar cells (PSCs). After the optimization, P126:Y6 and P127:Y6 attained overall power conversion efficiency of 15.07% and 12.27%, respectively. The higher PCE for the P126 than P127 is associated with the more efficient photon harvesting and photogenerated excitons, balanced charge transport, and low energy loss. Our results may help to design new polymers with a deeper highest occupied molecular orbital level that will be well-matched with non-fullerene acceptors.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
基于炭黑[1,2-b: 4,3-b': 6,7-c']三噻吩-8,12-二酮的新型宽带隙π共轭共聚物用于高性能非富勒烯聚合物太阳能电池,效率为15.07%
开发与窄禁带非富勒烯受体相匹配的高效宽禁带共聚物给体材料一直是聚合物太阳能电池的研究热点。本文设计并合成了两种新的D-A共聚物,通过包埋相同的炭素[1,2-b:4,3-b':6,7-c ']三噻吩-8,12-二酮(A3T)受体单元和不同的给体单元,即BDTTZ (P126)和bdth (P127)。这些共聚物具有350 ~ 680 nm的宽吸收和较深的HOMO能级。我们使用这两种共聚物作为供体和窄带隙非富勒烯受体Y6制备了体异质结聚合物太阳能电池(PSCs)。优化后,P126:Y6和P127:Y6的总功率转换效率分别达到15.07%和12.27%。P126的PCE比P127高,与更有效的光子捕获和光生激子、平衡的电荷输运和低能量损失有关。我们的结果可能有助于设计具有更深的最高占据分子轨道水平的新聚合物,这些聚合物将与非富勒烯受体很好地匹配。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Polymer
Polymer 化学-高分子科学
CiteScore
7.90
自引率
8.70%
发文量
959
审稿时长
32 days
期刊介绍: Polymer is an interdisciplinary journal dedicated to publishing innovative and significant advances in Polymer Physics, Chemistry and Technology. We welcome submissions on polymer hybrids, nanocomposites, characterisation and self-assembly. Polymer also publishes work on the technological application of polymers in energy and optoelectronics. The main scope is covered but not limited to the following core areas: Polymer Materials Nanocomposites and hybrid nanomaterials Polymer blends, films, fibres, networks and porous materials Physical Characterization Characterisation, modelling and simulation* of molecular and materials properties in bulk, solution, and thin films Polymer Engineering Advanced multiscale processing methods Polymer Synthesis, Modification and Self-assembly Including designer polymer architectures, mechanisms and kinetics, and supramolecular polymerization Technological Applications Polymers for energy generation and storage Polymer membranes for separation technology Polymers for opto- and microelectronics.
期刊最新文献
Functionalized Ionic Liquid Supported on Expandable Graphite for Achieving Efficient Fire Retardancy and High Thermal Conductivity in Thermoplastic Polyurethane Crystallization Regulation in Living Anionic Polymerization of 1,2-Dihydronaphthalene High-SiO2 Hydrogels with Intrinsic Antifreeze, Superior Strength, and Wear Resistance Polydimethylsiloxane Networks Integrated with Poly(ethylene oxide) Chains: Nanostructures, Reprocessing and Transformation into Solid Polymer Electrolytes Construction of High-Barrier, High-Strength EPDM Composites: Synergistic Optimization of Zinc methacrylate -Induced Covalent-Ionic Dual Network and Hydroxy Terminated Polybutadiene Plasticization
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1