{"title":"用于高效稳定有机太阳能电池的聚合物双层空穴传输层结构","authors":"","doi":"10.1016/j.joule.2024.06.013","DOIUrl":null,"url":null,"abstract":"<div><p>All-solution-processed organic photovoltaic (OPV) cells allow cost- and energy-effective fabrication methods for large-area devices. Despite significant progress on laboratory-scale devices, there is still a lack of interface materials that can be solution processed on top of the active layer, are compatible with novel non-fullerene acceptors (NFAs), and also provide sufficient long-term stability. We developed a novel interface layer concept, where alcohol-based organic polymer nanoparticles can be processed on top of a polymer-NFA active layer and doped to achieve a quasi-Ohmic hole contact. Moreover, poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) is processed as a second layer, forming a bilayer solution-processed hole transporting layer (HTL), providing an industrially relevant inverted architecture with a protective PEDOT:PSS layer on top. Most importantly, exceptional stability is observed. PM6:Y6 devices with the bilayer HTL are demonstrated to maintain 93% of their initial efficiency for 1,800 h under continuous solar cell operation at 60°C.</p></div>","PeriodicalId":343,"journal":{"name":"Joule","volume":null,"pages":null},"PeriodicalIF":38.6000,"publicationDate":"2024-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2542435124002897/pdfft?md5=cf339e8642c2fba921a3f5cf7b1f77a4&pid=1-s2.0-S2542435124002897-main.pdf","citationCount":"0","resultStr":"{\"title\":\"A polymer bilayer hole transporting layer architecture for high-efficiency and stable organic solar cells\",\"authors\":\"\",\"doi\":\"10.1016/j.joule.2024.06.013\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>All-solution-processed organic photovoltaic (OPV) cells allow cost- and energy-effective fabrication methods for large-area devices. Despite significant progress on laboratory-scale devices, there is still a lack of interface materials that can be solution processed on top of the active layer, are compatible with novel non-fullerene acceptors (NFAs), and also provide sufficient long-term stability. We developed a novel interface layer concept, where alcohol-based organic polymer nanoparticles can be processed on top of a polymer-NFA active layer and doped to achieve a quasi-Ohmic hole contact. Moreover, poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) is processed as a second layer, forming a bilayer solution-processed hole transporting layer (HTL), providing an industrially relevant inverted architecture with a protective PEDOT:PSS layer on top. Most importantly, exceptional stability is observed. PM6:Y6 devices with the bilayer HTL are demonstrated to maintain 93% of their initial efficiency for 1,800 h under continuous solar cell operation at 60°C.</p></div>\",\"PeriodicalId\":343,\"journal\":{\"name\":\"Joule\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":38.6000,\"publicationDate\":\"2024-09-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2542435124002897/pdfft?md5=cf339e8642c2fba921a3f5cf7b1f77a4&pid=1-s2.0-S2542435124002897-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Joule\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2542435124002897\",\"RegionNum\":1,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Joule","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2542435124002897","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
A polymer bilayer hole transporting layer architecture for high-efficiency and stable organic solar cells
All-solution-processed organic photovoltaic (OPV) cells allow cost- and energy-effective fabrication methods for large-area devices. Despite significant progress on laboratory-scale devices, there is still a lack of interface materials that can be solution processed on top of the active layer, are compatible with novel non-fullerene acceptors (NFAs), and also provide sufficient long-term stability. We developed a novel interface layer concept, where alcohol-based organic polymer nanoparticles can be processed on top of a polymer-NFA active layer and doped to achieve a quasi-Ohmic hole contact. Moreover, poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) is processed as a second layer, forming a bilayer solution-processed hole transporting layer (HTL), providing an industrially relevant inverted architecture with a protective PEDOT:PSS layer on top. Most importantly, exceptional stability is observed. PM6:Y6 devices with the bilayer HTL are demonstrated to maintain 93% of their initial efficiency for 1,800 h under continuous solar cell operation at 60°C.
期刊介绍:
Joule is a sister journal to Cell that focuses on research, analysis, and ideas related to sustainable energy. It aims to address the global challenge of the need for more sustainable energy solutions. Joule is a forward-looking journal that bridges disciplines and scales of energy research. It connects researchers and analysts working on scientific, technical, economic, policy, and social challenges related to sustainable energy. The journal covers a wide range of energy research, from fundamental laboratory studies on energy conversion and storage to global-level analysis. Joule aims to highlight and amplify the implications, challenges, and opportunities of novel energy research for different groups in the field.