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揭示连接体对高性能聚合物太阳能电池中寡聚受体构象的影响。

Unveiling the Influence of Linkers on Conformations of Oligomeric Acceptors for High-Performance Polymer Solar Cells.

作者信息

Wu Jingnan, Sun Fengbo, Wang Xunchang, Chen Qiaonan, Franco Leandro R, Zheng Xufan, Araujo C Moyses, Yang Renqiang, Yu Donghong, Wang Ergang

机构信息

Department of Chemistry and Chemical Engineering, Chalmers University of Technology, Göteborg, SE-412 96, Sweden.

Department of Chemistry and Bioscience, Aalborg University, Aalborg, DK-9220, Denmark.

出版信息

Adv Sci (Weinh). 2024 Oct;11(40):e2406772. doi: 10.1002/advs.202406772. Epub 2024 Aug 29.

DOI:10.1002/advs.202406772
PMID:39206722
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11515919/
Abstract

Conformational isomerism of organic photovoltaic materials has a profound impact on their molecular packing and therefore performance of polymer solar cells (PSCs). However, the conformations of oligomeric acceptors (OAs) are mostly predicted by simulations rather than experimental determinations. Herein, the stereochemical S-shaped structure of two dimeric-type acceptor molecules, V-DYIC and V-DYIC-4F, is first confirmed with different end groups (IC for V-DYIC and IC-2F for V-DYIC-4F), incorporating vinylene linkage for connecting the distinct state-of-the-art small molecule acceptor Y-segments. Through the synthetic control of fluorination sites adjacent to the vinyl-linker, S-shaped the conformation by NMR experiments is validated. Compared to the O-shaped dimer, S-shaped conformation results in enhanced lamellar order and reduced nonradiative recombination losses. The optimal acceptor, V-DYIC-4F, achieved a champion efficiency of 18.10% with the lowest energy loss of 0.556 eV in its devices paired with PM6 due to their efficient carrier transport, and suppressed recombination compared to other devices, being attributed to the synergistic effect of conformation and end group fluorination. The insights gained in this work contribute valuable knowledge of both synthetic control and structural determination of OAs, providing strategic design guidelines for the future development of dimeric acceptors toward high-efficiency PSCs.

摘要

有机光伏材料的构象异构对其分子堆积以及聚合物太阳能电池(PSC)的性能有着深远影响。然而,寡聚受体(OA)的构象大多是通过模拟预测,而非实验测定。在此,首次通过不同的端基(V-DYIC的IC和V-DYIC-4F的IC-2F)证实了两种二聚体型受体分子V-DYIC和V-DYIC-4F的立体化学S形结构,引入亚乙烯基连接以连接不同的先进小分子受体Y段。通过对与乙烯基连接体相邻的氟化位点进行合成控制,通过核磁共振实验验证了S形构象。与O形二聚体相比,S形构象导致层状有序性增强,非辐射复合损失降低。最优受体V-DYIC-4F在与PM6配对的器件中实现了18.10%的最佳效率,最低能量损失为0.556 eV,这归因于其高效的载流子传输,且与其他器件相比复合受到抑制,这归因于构象和端基氟化的协同效应。这项工作中获得的见解为OA的合成控制和结构测定提供了有价值的知识,为二聚体受体未来向高效PSC发展提供了战略设计指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e494/11515919/43e656e1c9ce/ADVS-11-2406772-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e494/11515919/8f01294b6076/ADVS-11-2406772-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e494/11515919/8ad592e94042/ADVS-11-2406772-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e494/11515919/97bdb94c8cc2/ADVS-11-2406772-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e494/11515919/1347142034aa/ADVS-11-2406772-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e494/11515919/43e656e1c9ce/ADVS-11-2406772-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e494/11515919/8f01294b6076/ADVS-11-2406772-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e494/11515919/8ad592e94042/ADVS-11-2406772-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e494/11515919/97bdb94c8cc2/ADVS-11-2406772-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e494/11515919/1347142034aa/ADVS-11-2406772-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e494/11515919/43e656e1c9ce/ADVS-11-2406772-g004.jpg

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本文引用的文献

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Strengthening the Hetero-Molecular Interactions in Giant Dimeric Acceptors Enables Efficient Organic Solar Cells.增强巨型二聚体受体中的异质分子相互作用可实现高效有机太阳能电池。
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Delayed Crystallization Kinetics Allowing High-Efficiency All-Polymer Photovoltaics with Superior Upscaled Manufacturing.
延迟结晶动力学助力实现具有卓越放大制造能力的高效全聚合物光伏器件。
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