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硅和锗功能化苝二酰亚胺:合成、光电性质及其作为有机太阳能电池中非富勒烯受体的应用

Silicon- and Germanium-Functionalized Perylene Diimides: Synthesis, Optoelectronic Properties, and Their Application as Non-fullerene Acceptors in Organic Solar Cells.

作者信息

Schlemmer Bettina, Sauermoser Aileen, Holler Sarah, Zuccalà Elena, Ehmann Birgit, Reinfelds Matiss, Fischer Roland C, Amenitsch Heinz, Marin-Beloqui Jose M, Ludvíková Lucie, Slanina Tomáš, Haas Michael, Rath Thomas, Trimmel Gregor

机构信息

Institute for Chemistry and Technology of Materials, NAWI Graz, Graz University of Technology, Stremayrgasse 9, 8010, Graz, Austria.

Institute of Inorganic Chemistry, NAWI Graz, Graz University of Technology, Stremayrgasse 9, 8010, Graz, Austria.

出版信息

Chemistry. 2023 Oct 13;29(57):e202301337. doi: 10.1002/chem.202301337. Epub 2023 Aug 28.

DOI:10.1002/chem.202301337
PMID:37419861
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10946824/
Abstract

Organic solar cells have been continuously studied and developed through the last decades. A major step in their development was the introduction of fused-ring non-fullerene electron acceptors. Yet, beside their high efficiency, they suffer from complex synthesis and stability issues. Perylene-based non-fullerene acceptors, in contrast, can be prepared in only a few steps and display good photochemical and thermal stability. Herein, we introduce four monomeric perylene diimide acceptors obtained in a three-step synthesis. In these molecules, the semimetals silicon and germanium were added in the bay position, on one or both sides of the molecules, resulting in asymmetric and symmetric compounds with a red-shifted absorption compared to unsubstituted perylene diimide. Introducing two germanium atoms improved the crystallinity and charge carrier mobility in the blend with the conjugated polymer PM6. In addition, charge carrier separation is significantly influenced by the high crystallinity of this blend, as shown by transient absorption spectroscopy. As a result, the solar cells reached a power conversion efficiency of 5.38 %, which is one of the highest efficiencies of monomeric perylene diimide-based solar cells recorded to date.

摘要

在过去几十年里,有机太阳能电池一直在持续研究和发展。其发展的一个重要阶段是引入了稠环非富勒烯电子受体。然而,尽管它们效率高,但存在合成复杂和稳定性问题。相比之下,基于苝的非富勒烯受体只需几步就能制备,并且具有良好的光化学和热稳定性。在此,我们介绍通过三步合成得到的四种单体苝二酰亚胺受体。在这些分子中,半金属硅和锗被添加到分子一侧或两侧的湾区位置,与未取代的苝二酰亚胺相比,形成了具有红移吸收的不对称和对称化合物。引入两个锗原子提高了与共轭聚合物PM6共混物中的结晶度和电荷载流子迁移率。此外,如瞬态吸收光谱所示,电荷载流子分离受到该共混物高结晶度的显著影响。结果,太阳能电池的功率转换效率达到了5.38%,这是迄今为止基于单体苝二酰亚胺的太阳能电池记录的最高效率之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1024/10946824/60663fec9bb7/CHEM-29-0-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1024/10946824/c1c7ec904e31/CHEM-29-0-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1024/10946824/9dce83f250f4/CHEM-29-0-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1024/10946824/d0bb80121b7a/CHEM-29-0-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1024/10946824/db9b4dcb3bb0/CHEM-29-0-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1024/10946824/e89ad3d66609/CHEM-29-0-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1024/10946824/7ddadcfee2ac/CHEM-29-0-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1024/10946824/b0d394e18cec/CHEM-29-0-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1024/10946824/b8c2f19dd160/CHEM-29-0-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1024/10946824/60663fec9bb7/CHEM-29-0-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1024/10946824/c1c7ec904e31/CHEM-29-0-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1024/10946824/9dce83f250f4/CHEM-29-0-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1024/10946824/d0bb80121b7a/CHEM-29-0-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1024/10946824/db9b4dcb3bb0/CHEM-29-0-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1024/10946824/e89ad3d66609/CHEM-29-0-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1024/10946824/7ddadcfee2ac/CHEM-29-0-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1024/10946824/b0d394e18cec/CHEM-29-0-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1024/10946824/b8c2f19dd160/CHEM-29-0-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1024/10946824/60663fec9bb7/CHEM-29-0-g001.jpg

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