Yahui Bai, Linwei Xie, Zhihui Lin, Qi Ai, Fuwen Zhao, Dan He
{"title":"Optimizing Miscibility for Enhanced Photovoltaic Performance of Non-Fused Ring Electron Acceptors through Side-Chain Engineering","authors":"Yahui Bai, Linwei Xie, Zhihui Lin, Qi Ai, Fuwen Zhao, Dan He","doi":"10.1039/d5cp00267b","DOIUrl":null,"url":null,"abstract":"Non-fused ring electron acceptors (NFREAs), notable for their simple and economical synthesis processes, play a pivotal role in the practical deployment of organic solar cells (OSCs). However, the power conversion efficiency (PCE) of NFREAs based devices lags behind that of fused ring electron acceptors, because of the inferior charge transport and severe charge recombination in donor:NFREAs blend films. In this study, we synthesized two novel NFREAs—A1C4-Cl and A1C6-Cl—featuring different alkyl side-chain lengths to optimize the miscibility between the donor and NFREAs for ideal morphology, taking into consideration that morphology of donor:NFREAs blend films has significant influence on charge transport and recombination. The PBDB-T:A1C6-Cl based OSC exhibits better miscibility and more favourable phase separation, resulting in enhanced charge carrier mobilities and suppressed trap-assisted recombination. These improvements lead to a significant increase in short-circuit current density (JSC) and fill factor (FF), culminating in a PCE of 12.11% compared to the PBDB-T:A1C4-Cl based devices. Our findings offer an effective approach to modulating the miscibility between donors and NFREAs, thereby enhancing the PCE of OSCs through the fine-tuning of alkyl side-chain lengths.","PeriodicalId":99,"journal":{"name":"Physical Chemistry Chemical Physics","volume":"12 1","pages":""},"PeriodicalIF":2.9000,"publicationDate":"2025-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physical Chemistry Chemical Physics","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5cp00267b","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Optimizing Miscibility for Enhanced Photovoltaic Performance of Non-Fused Ring Electron Acceptors through Side-Chain Engineering
Non-fused ring electron acceptors (NFREAs), notable for their simple and economical synthesis processes, play a pivotal role in the practical deployment of organic solar cells (OSCs). However, the power conversion efficiency (PCE) of NFREAs based devices lags behind that of fused ring electron acceptors, because of the inferior charge transport and severe charge recombination in donor:NFREAs blend films. In this study, we synthesized two novel NFREAs—A1C4-Cl and A1C6-Cl—featuring different alkyl side-chain lengths to optimize the miscibility between the donor and NFREAs for ideal morphology, taking into consideration that morphology of donor:NFREAs blend films has significant influence on charge transport and recombination. The PBDB-T:A1C6-Cl based OSC exhibits better miscibility and more favourable phase separation, resulting in enhanced charge carrier mobilities and suppressed trap-assisted recombination. These improvements lead to a significant increase in short-circuit current density (JSC) and fill factor (FF), culminating in a PCE of 12.11% compared to the PBDB-T:A1C4-Cl based devices. Our findings offer an effective approach to modulating the miscibility between donors and NFREAs, thereby enhancing the PCE of OSCs through the fine-tuning of alkyl side-chain lengths.
期刊介绍:
Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions.
The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.