{"title":"通过微调分子结晶和成膜动力学用于高效有机太阳能电池的低成本熔合环电子受体。","authors":"Wenkui Wei,Xiyue Yuan,Xia Zhou,Yao Li,Seunglok Lee,Jinqun Xu,Yue Zhang,Haozhe Feng,Qiuju Jiang,Jiaying Wu,Changduk Yang,Xiaotao Hao,Fei Huang,Yong Cao,Chunhui Duan","doi":"10.1002/anie.202517485","DOIUrl":null,"url":null,"abstract":"Achieving high power conversion efficiencies (PCEs) with low-cost active layer materials is of vital importance for organic solar cell (OSC) commercialization. However, the PCEs afforded by currently reported low-cost electron acceptors remain substantially limited. Herein, we report the regulation of molecular crystallization and film formation kinetics of the low-cost electron acceptors with A-DA'D-A-type pentacyclic fused-ring structures and achieved an impressive PCE of 18.04% and a tiptop figure-of-merit (FOM) of 0.363, representing the best-known values for OSCs. Single crystal X-ray diffraction studies indicate that the long and flexible side chain on the central core could hinder the unfavorable dimer formation of electron acceptors and lead to three-dimensional network packing, which is critical for exciton diffusion and charge transport. Moreover, the in situ optical spectroscopy revealed that the side chain elongation of the electron acceptor could slow the film formation kinetics of the small molecular acceptor while accelerating those of the polymer donor, which is conducive to forming bi-continuous interpenetrating fibril networks with better intermixing. This work demonstrates that low-cost, simple-structured fused-ring electron acceptors hold a bright future in the OSC commercialization.","PeriodicalId":125,"journal":{"name":"Angewandte Chemie International Edition","volume":"114 1","pages":"e202517485"},"PeriodicalIF":16.9000,"publicationDate":"2025-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Low-Cost Fused-Ring Electron Acceptors for Efficient Organic Solar Cells by Fine-Tuning Molecular Crystallization and Film Formation Kinetics.\",\"authors\":\"Wenkui Wei,Xiyue Yuan,Xia Zhou,Yao Li,Seunglok Lee,Jinqun Xu,Yue Zhang,Haozhe Feng,Qiuju Jiang,Jiaying Wu,Changduk Yang,Xiaotao Hao,Fei Huang,Yong Cao,Chunhui Duan\",\"doi\":\"10.1002/anie.202517485\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Achieving high power conversion efficiencies (PCEs) with low-cost active layer materials is of vital importance for organic solar cell (OSC) commercialization. However, the PCEs afforded by currently reported low-cost electron acceptors remain substantially limited. Herein, we report the regulation of molecular crystallization and film formation kinetics of the low-cost electron acceptors with A-DA'D-A-type pentacyclic fused-ring structures and achieved an impressive PCE of 18.04% and a tiptop figure-of-merit (FOM) of 0.363, representing the best-known values for OSCs. Single crystal X-ray diffraction studies indicate that the long and flexible side chain on the central core could hinder the unfavorable dimer formation of electron acceptors and lead to three-dimensional network packing, which is critical for exciton diffusion and charge transport. Moreover, the in situ optical spectroscopy revealed that the side chain elongation of the electron acceptor could slow the film formation kinetics of the small molecular acceptor while accelerating those of the polymer donor, which is conducive to forming bi-continuous interpenetrating fibril networks with better intermixing. This work demonstrates that low-cost, simple-structured fused-ring electron acceptors hold a bright future in the OSC commercialization.\",\"PeriodicalId\":125,\"journal\":{\"name\":\"Angewandte Chemie International Edition\",\"volume\":\"114 1\",\"pages\":\"e202517485\"},\"PeriodicalIF\":16.9000,\"publicationDate\":\"2025-10-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Angewandte Chemie International Edition\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1002/anie.202517485\",\"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":"Angewandte Chemie International Edition","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/anie.202517485","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
利用低成本的活性层材料实现高功率转换效率(pce)对于有机太阳能电池(OSC)的商业化至关重要。然而,目前报道的低成本电子受体提供的pce仍然非常有限。在此,我们报道了具有a - da ' d- a型五环融合环结构的低成本电子受体的分子结晶和成膜动力学的调控,并获得了令人印象印象的PCE为18.04%和最高价值图(FOM)为0.363,代表了osc的最知名值。单晶x射线衍射研究表明,中心核上的长而灵活的侧链可以阻碍电子受体的不利二聚体形成,并导致三维网络堆积,这对激子扩散和电荷输运至关重要。原位光谱学分析表明,电子受体侧链的伸长可以减缓小分子受体的成膜动力学,而加速聚合物给体的成膜动力学,有利于形成双连续互穿的纤维网络,并具有更好的混合性能。这项工作表明,低成本、结构简单的融合环电子受体在OSC商业化中具有光明的前景。
Low-Cost Fused-Ring Electron Acceptors for Efficient Organic Solar Cells by Fine-Tuning Molecular Crystallization and Film Formation Kinetics.
Achieving high power conversion efficiencies (PCEs) with low-cost active layer materials is of vital importance for organic solar cell (OSC) commercialization. However, the PCEs afforded by currently reported low-cost electron acceptors remain substantially limited. Herein, we report the regulation of molecular crystallization and film formation kinetics of the low-cost electron acceptors with A-DA'D-A-type pentacyclic fused-ring structures and achieved an impressive PCE of 18.04% and a tiptop figure-of-merit (FOM) of 0.363, representing the best-known values for OSCs. Single crystal X-ray diffraction studies indicate that the long and flexible side chain on the central core could hinder the unfavorable dimer formation of electron acceptors and lead to three-dimensional network packing, which is critical for exciton diffusion and charge transport. Moreover, the in situ optical spectroscopy revealed that the side chain elongation of the electron acceptor could slow the film formation kinetics of the small molecular acceptor while accelerating those of the polymer donor, which is conducive to forming bi-continuous interpenetrating fibril networks with better intermixing. This work demonstrates that low-cost, simple-structured fused-ring electron acceptors hold a bright future in the OSC commercialization.
期刊介绍:
Angewandte Chemie, a journal of the German Chemical Society (GDCh), maintains a leading position among scholarly journals in general chemistry with an impressive Impact Factor of 16.6 (2022 Journal Citation Reports, Clarivate, 2023). Published weekly in a reader-friendly format, it features new articles almost every day. Established in 1887, Angewandte Chemie is a prominent chemistry journal, offering a dynamic blend of Review-type articles, Highlights, Communications, and Research Articles on a weekly basis, making it unique in the field.