{"title":"高效稳定倒置钙钛矿太阳能电池的全共轭共自组装单层膜","authors":"Yuanzhong Liu, Xin Yang, Xinliang Ding, Jiarong Wang, Weitai Xu, Xiaoting Wang, Liujiang Zhang, Yiran Yan, Jia Wang, Yanna Hou, Lin Yang, Tianjiao Chu, Qinglong Jiang, Xiangrong Zhu, Ziyang Hu, Bin Kan, Xingyu Gao, Qiang Fu, Liyou Yang, Zhicai Chen, Shiyang Shao, Linfeng Lu, Xiaofei Ji","doi":"10.1002/smll.202502367","DOIUrl":null,"url":null,"abstract":"<p>[4-(3,6-dimethyl-9H-carbazol-9-yl)butyl]phosphonic acid (Me-4PACz) consistently exhibits inhomogeneous distribution on the substrate, which makes it a challenge for the growth of high-quality perovskite film, resulting in undesired interfacial losses at buried interfaces. Moreover, the flexible alkyl chains of Me-4PACz are not conducive to intermolecular interactions and hinder charge flow. Here, a novel molecule with 4-Methoxy-N-(4-methoxyphenyl)-N-phenylaniline (TPA) and carbazole backbone, named CzTPA is designed, which constituted Co-SAM with Me-4PACz. The two carboxyls on the end of carbazole will act as an anchoring group to cover the inadequate coverage of Me-4PACz on the NiO<sub>x</sub>. The methoxy group on the TPA can passivation the uncoordinated Pb<sup>2+</sup> at the perovskite buried interface by the interaction of Pb─O. Additionally, the Me-4PACz can be restrained self-aggregation by interacting with the TPA group of CzTPA. The cooperation of CzTPA realizes the more homogeneous distribution of Me-4PACz on the NiO<sub>x</sub>, efficient charge transport, and minimize buried interfacial defects. Accordingly, the CzTPA modification can significantly enhance the efficiency of 1.54-eV PSCs from 23.53% to 25.66% and sustain 91.4% of its original efficiency after 1992 h under continuous illumination at 65 °C. More importantly, a 1.68 eV of wide-bandgap PSC achieved a PCE of 22.75% with good photostability.</p>","PeriodicalId":228,"journal":{"name":"Small","volume":"21 17","pages":""},"PeriodicalIF":12.1000,"publicationDate":"2025-03-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Fully Conjugated Co-Self-Assembled Monolayers for Efficient and Stable Inverted Perovskite Solar Cells\",\"authors\":\"Yuanzhong Liu, Xin Yang, Xinliang Ding, Jiarong Wang, Weitai Xu, Xiaoting Wang, Liujiang Zhang, Yiran Yan, Jia Wang, Yanna Hou, Lin Yang, Tianjiao Chu, Qinglong Jiang, Xiangrong Zhu, Ziyang Hu, Bin Kan, Xingyu Gao, Qiang Fu, Liyou Yang, Zhicai Chen, Shiyang Shao, Linfeng Lu, Xiaofei Ji\",\"doi\":\"10.1002/smll.202502367\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>[4-(3,6-dimethyl-9H-carbazol-9-yl)butyl]phosphonic acid (Me-4PACz) consistently exhibits inhomogeneous distribution on the substrate, which makes it a challenge for the growth of high-quality perovskite film, resulting in undesired interfacial losses at buried interfaces. Moreover, the flexible alkyl chains of Me-4PACz are not conducive to intermolecular interactions and hinder charge flow. Here, a novel molecule with 4-Methoxy-N-(4-methoxyphenyl)-N-phenylaniline (TPA) and carbazole backbone, named CzTPA is designed, which constituted Co-SAM with Me-4PACz. The two carboxyls on the end of carbazole will act as an anchoring group to cover the inadequate coverage of Me-4PACz on the NiO<sub>x</sub>. The methoxy group on the TPA can passivation the uncoordinated Pb<sup>2+</sup> at the perovskite buried interface by the interaction of Pb─O. Additionally, the Me-4PACz can be restrained self-aggregation by interacting with the TPA group of CzTPA. The cooperation of CzTPA realizes the more homogeneous distribution of Me-4PACz on the NiO<sub>x</sub>, efficient charge transport, and minimize buried interfacial defects. Accordingly, the CzTPA modification can significantly enhance the efficiency of 1.54-eV PSCs from 23.53% to 25.66% and sustain 91.4% of its original efficiency after 1992 h under continuous illumination at 65 °C. More importantly, a 1.68 eV of wide-bandgap PSC achieved a PCE of 22.75% with good photostability.</p>\",\"PeriodicalId\":228,\"journal\":{\"name\":\"Small\",\"volume\":\"21 17\",\"pages\":\"\"},\"PeriodicalIF\":12.1000,\"publicationDate\":\"2025-03-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Small\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/smll.202502367\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Small","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/smll.202502367","RegionNum":2,"RegionCategory":"材料科学","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
[4-(3,6-二甲基- 9h -咔唑-9-基)丁基]膦酸(Me-4PACz)在衬底上的分布一直不均匀,这给高质量钙钛矿薄膜的生长带来了挑战,导致埋在界面处的界面损失。此外,Me-4PACz的柔性烷基链不利于分子间相互作用,阻碍电荷流动。本文设计了一种以4-甲氧基- n -(4-甲氧基苯基)- n -苯基苯胺(TPA)和咔唑为骨架的新型分子CzTPA,与Me-4PACz构成Co-SAM。咔唑末端的两个羧基将作为一个锚定基团,以覆盖Me-4PACz在NiOx上的不充分覆盖。TPA上的甲氧基可以通过Pb─O的相互作用钝化钙钛矿界面处的未配位Pb2+。此外,Me-4PACz可以通过与CzTPA的TPA基团相互作用抑制自聚集。通过与CzTPA的合作,实现了Me-4PACz在NiOx上的均匀分布,高效的电荷输运,最大限度地减少了埋藏界面缺陷。因此,在65°C的连续光照条件下,经过CzTPA修饰后,1.54 ev PSCs的效率从23.53%显著提高到25.66%,并在1992 h后保持原来效率的91.4%。更重要的是,1.68 eV的宽禁带PSC的PCE为22.75%,具有良好的光稳定性。
Fully Conjugated Co-Self-Assembled Monolayers for Efficient and Stable Inverted Perovskite Solar Cells
[4-(3,6-dimethyl-9H-carbazol-9-yl)butyl]phosphonic acid (Me-4PACz) consistently exhibits inhomogeneous distribution on the substrate, which makes it a challenge for the growth of high-quality perovskite film, resulting in undesired interfacial losses at buried interfaces. Moreover, the flexible alkyl chains of Me-4PACz are not conducive to intermolecular interactions and hinder charge flow. Here, a novel molecule with 4-Methoxy-N-(4-methoxyphenyl)-N-phenylaniline (TPA) and carbazole backbone, named CzTPA is designed, which constituted Co-SAM with Me-4PACz. The two carboxyls on the end of carbazole will act as an anchoring group to cover the inadequate coverage of Me-4PACz on the NiOx. The methoxy group on the TPA can passivation the uncoordinated Pb2+ at the perovskite buried interface by the interaction of Pb─O. Additionally, the Me-4PACz can be restrained self-aggregation by interacting with the TPA group of CzTPA. The cooperation of CzTPA realizes the more homogeneous distribution of Me-4PACz on the NiOx, efficient charge transport, and minimize buried interfacial defects. Accordingly, the CzTPA modification can significantly enhance the efficiency of 1.54-eV PSCs from 23.53% to 25.66% and sustain 91.4% of its original efficiency after 1992 h under continuous illumination at 65 °C. More importantly, a 1.68 eV of wide-bandgap PSC achieved a PCE of 22.75% with good photostability.
期刊介绍:
Small serves as an exceptional platform for both experimental and theoretical studies in fundamental and applied interdisciplinary research at the nano- and microscale. The journal offers a compelling mix of peer-reviewed Research Articles, Reviews, Perspectives, and Comments.
With a remarkable 2022 Journal Impact Factor of 13.3 (Journal Citation Reports from Clarivate Analytics, 2023), Small remains among the top multidisciplinary journals, covering a wide range of topics at the interface of materials science, chemistry, physics, engineering, medicine, and biology.
Small's readership includes biochemists, biologists, biomedical scientists, chemists, engineers, information technologists, materials scientists, physicists, and theoreticians alike.