Ahmed I. A. Soliman, Yiran Zheng, Guofeng You, Lin Zhang, Yiqing Zhang, Haotian Wu, Zhichuan Wang, Weifei Fu, Hongzheng Chen
{"title":"稳定倒钙钛矿太阳能电池抗溶剂性提高的自组装双层膜","authors":"Ahmed I. A. Soliman, Yiran Zheng, Guofeng You, Lin Zhang, Yiqing Zhang, Haotian Wu, Zhichuan Wang, Weifei Fu, Hongzheng Chen","doi":"10.1002/smll.202506226","DOIUrl":null,"url":null,"abstract":"The self-assembled monolayer (SAM) molecules on ITO or metal oxide transporting layers tend to desorb during perovskite film processing and device operation, leading to reduced power conversion efficiency (PCE) and device degradation. Developing effective strategies to stabilize SAMs at interfaces is therefore crucial for further improving the performance and stability of SAM-based perovskite solar cells (PVSCs). Here, a facile method is developed to construct robust self-assembled bilayers (SABs) by depositing cross-linkable organosilanes, <i>n</i>-propyltrimethoxysilane (PTMS) and (3-mercaptopropyl)trimethoxysilane (MPTMS), onto the widely used Me-4PACz SAM for NiO<sub>x</sub> modification. Me-4PACz enables excellent hole extraction, suppresses interfacial reactions and recombination, while the cross-linked organosilane network forms a robust protective layer that prevents the solvent-induced SAM desorption and fills molecular voids, yielding a more compact and stable interface. In addition, the thiol group in MPTMS can strongly interact with the undercoordinated Pb<sup>2+</sup> at the buried interface of perovskite, further mitigating interfacial defects. Consequently, NiO<sub>x</sub>/Me-4PACz/MPTMS based PVSCs achieve a high PCE of 24.9% with a <i>T</i><sub>80</sub> lifetime of 475 h under continuous 1 sun equivalent illumination in air, compared to 23.3% and tens of hours for NiO<sub>x</sub>/Me-4PACz-based control device. This work provides important insights into designing robust interfaces for high-performance and highly stable PVSCs.","PeriodicalId":228,"journal":{"name":"Small","volume":"21 1","pages":""},"PeriodicalIF":12.1000,"publicationDate":"2025-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Self-Assembled Bilayers with Improved Solvent Resistance for Stable Inverted Perovskite Solar Cells\",\"authors\":\"Ahmed I. A. Soliman, Yiran Zheng, Guofeng You, Lin Zhang, Yiqing Zhang, Haotian Wu, Zhichuan Wang, Weifei Fu, Hongzheng Chen\",\"doi\":\"10.1002/smll.202506226\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The self-assembled monolayer (SAM) molecules on ITO or metal oxide transporting layers tend to desorb during perovskite film processing and device operation, leading to reduced power conversion efficiency (PCE) and device degradation. Developing effective strategies to stabilize SAMs at interfaces is therefore crucial for further improving the performance and stability of SAM-based perovskite solar cells (PVSCs). Here, a facile method is developed to construct robust self-assembled bilayers (SABs) by depositing cross-linkable organosilanes, <i>n</i>-propyltrimethoxysilane (PTMS) and (3-mercaptopropyl)trimethoxysilane (MPTMS), onto the widely used Me-4PACz SAM for NiO<sub>x</sub> modification. Me-4PACz enables excellent hole extraction, suppresses interfacial reactions and recombination, while the cross-linked organosilane network forms a robust protective layer that prevents the solvent-induced SAM desorption and fills molecular voids, yielding a more compact and stable interface. In addition, the thiol group in MPTMS can strongly interact with the undercoordinated Pb<sup>2+</sup> at the buried interface of perovskite, further mitigating interfacial defects. Consequently, NiO<sub>x</sub>/Me-4PACz/MPTMS based PVSCs achieve a high PCE of 24.9% with a <i>T</i><sub>80</sub> lifetime of 475 h under continuous 1 sun equivalent illumination in air, compared to 23.3% and tens of hours for NiO<sub>x</sub>/Me-4PACz-based control device. 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Self-Assembled Bilayers with Improved Solvent Resistance for Stable Inverted Perovskite Solar Cells
The self-assembled monolayer (SAM) molecules on ITO or metal oxide transporting layers tend to desorb during perovskite film processing and device operation, leading to reduced power conversion efficiency (PCE) and device degradation. Developing effective strategies to stabilize SAMs at interfaces is therefore crucial for further improving the performance and stability of SAM-based perovskite solar cells (PVSCs). Here, a facile method is developed to construct robust self-assembled bilayers (SABs) by depositing cross-linkable organosilanes, n-propyltrimethoxysilane (PTMS) and (3-mercaptopropyl)trimethoxysilane (MPTMS), onto the widely used Me-4PACz SAM for NiOx modification. Me-4PACz enables excellent hole extraction, suppresses interfacial reactions and recombination, while the cross-linked organosilane network forms a robust protective layer that prevents the solvent-induced SAM desorption and fills molecular voids, yielding a more compact and stable interface. In addition, the thiol group in MPTMS can strongly interact with the undercoordinated Pb2+ at the buried interface of perovskite, further mitigating interfacial defects. Consequently, NiOx/Me-4PACz/MPTMS based PVSCs achieve a high PCE of 24.9% with a T80 lifetime of 475 h under continuous 1 sun equivalent illumination in air, compared to 23.3% and tens of hours for NiOx/Me-4PACz-based control device. This work provides important insights into designing robust interfaces for high-performance and highly stable PVSCs.
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.