{"title":"低温碳基钙钛矿太阳能电池中聚合物增强活性层结晶","authors":"Shih-Han Huang, Yu-Hsiang Chen, Hou-Chin Cha, Damian Glowienka, Ming-Chung Wu* and Yu-Ching Huang*, ","doi":"10.1021/acs.energyfuels.4c0389810.1021/acs.energyfuels.4c03898","DOIUrl":null,"url":null,"abstract":"<p >High-efficiency perovskite solar cells (PSCs) are emerging as a promising next-generation, low-cost, photovoltaic technology. A key advantage of PSCs is their compatibility with diverse manufacturing techniques, enabling the pursuit of low-cost, stable PSCs. Carbon electrodes, known for their scalability, chemical inertness, and ease of processing through screen printing, have recently seen the development of low-temperature carbon electrodes with high conductivity for use in PSCs. However, optimizing low-temperature carbon-based PSCs (LTC-PSCs), particularly improving the interface between the perovskite and carbon electrodes, remains a significant challenge. In this study, poly(3-hexylthiophene-2,5-diyl) (P3HT) was employed as an additive and a hole-transporting layer (HTL) in LTC-PSCs with low-temperature screen-printing carbon electrodes. The incorporation of P3HT in antisolvent improved the perovskite/carbon interface, reducing the defect density of the perovskite layer. This resulted in a significant average power conversion efficiency (PCE) improvement of 11%. The LTC-PSCs achieved a PCE of 10.90% and demonstrated exceptional stability, retaining 90% of initial PCE after 1200 h under ambient air. This research highlights the potential of LTC-PSCs as low-cost strategies for the commercialization of PSCs.</p>","PeriodicalId":35,"journal":{"name":"Energy & Fuels","volume":"39 2","pages":"1401–1408 1401–1408"},"PeriodicalIF":5.3000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Polymer-Enhanced Active Layer Crystallization in Low-Temperature Carbon-Based Perovskite Solar Cells\",\"authors\":\"Shih-Han Huang, Yu-Hsiang Chen, Hou-Chin Cha, Damian Glowienka, Ming-Chung Wu* and Yu-Ching Huang*, \",\"doi\":\"10.1021/acs.energyfuels.4c0389810.1021/acs.energyfuels.4c03898\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >High-efficiency perovskite solar cells (PSCs) are emerging as a promising next-generation, low-cost, photovoltaic technology. A key advantage of PSCs is their compatibility with diverse manufacturing techniques, enabling the pursuit of low-cost, stable PSCs. Carbon electrodes, known for their scalability, chemical inertness, and ease of processing through screen printing, have recently seen the development of low-temperature carbon electrodes with high conductivity for use in PSCs. However, optimizing low-temperature carbon-based PSCs (LTC-PSCs), particularly improving the interface between the perovskite and carbon electrodes, remains a significant challenge. In this study, poly(3-hexylthiophene-2,5-diyl) (P3HT) was employed as an additive and a hole-transporting layer (HTL) in LTC-PSCs with low-temperature screen-printing carbon electrodes. The incorporation of P3HT in antisolvent improved the perovskite/carbon interface, reducing the defect density of the perovskite layer. This resulted in a significant average power conversion efficiency (PCE) improvement of 11%. The LTC-PSCs achieved a PCE of 10.90% and demonstrated exceptional stability, retaining 90% of initial PCE after 1200 h under ambient air. This research highlights the potential of LTC-PSCs as low-cost strategies for the commercialization of PSCs.</p>\",\"PeriodicalId\":35,\"journal\":{\"name\":\"Energy & Fuels\",\"volume\":\"39 2\",\"pages\":\"1401–1408 1401–1408\"},\"PeriodicalIF\":5.3000,\"publicationDate\":\"2025-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Energy & Fuels\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.energyfuels.4c03898\",\"RegionNum\":3,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ENERGY & FUELS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Energy & Fuels","FirstCategoryId":"5","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.energyfuels.4c03898","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENERGY & FUELS","Score":null,"Total":0}
Polymer-Enhanced Active Layer Crystallization in Low-Temperature Carbon-Based Perovskite Solar Cells
High-efficiency perovskite solar cells (PSCs) are emerging as a promising next-generation, low-cost, photovoltaic technology. A key advantage of PSCs is their compatibility with diverse manufacturing techniques, enabling the pursuit of low-cost, stable PSCs. Carbon electrodes, known for their scalability, chemical inertness, and ease of processing through screen printing, have recently seen the development of low-temperature carbon electrodes with high conductivity for use in PSCs. However, optimizing low-temperature carbon-based PSCs (LTC-PSCs), particularly improving the interface between the perovskite and carbon electrodes, remains a significant challenge. In this study, poly(3-hexylthiophene-2,5-diyl) (P3HT) was employed as an additive and a hole-transporting layer (HTL) in LTC-PSCs with low-temperature screen-printing carbon electrodes. The incorporation of P3HT in antisolvent improved the perovskite/carbon interface, reducing the defect density of the perovskite layer. This resulted in a significant average power conversion efficiency (PCE) improvement of 11%. The LTC-PSCs achieved a PCE of 10.90% and demonstrated exceptional stability, retaining 90% of initial PCE after 1200 h under ambient air. This research highlights the potential of LTC-PSCs as low-cost strategies for the commercialization of PSCs.
期刊介绍:
Energy & Fuels publishes reports of research in the technical area defined by the intersection of the disciplines of chemistry and chemical engineering and the application domain of non-nuclear energy and fuels. This includes research directed at the formation of, exploration for, and production of fossil fuels and biomass; the properties and structure or molecular composition of both raw fuels and refined products; the chemistry involved in the processing and utilization of fuels; fuel cells and their applications; and the analytical and instrumental techniques used in investigations of the foregoing areas.