{"title":"稳定定向蒸发宽禁带钙钛矿太阳能电池的中间相演化。","authors":"Zijing Dong,Jingcong Hu,Xiao Guo,Zhuojie Shi,Haijie Chen,Yunluo Wang,Ran Luo,Julian A Steele,Zachary Degnan,Eduardo Solano,Qilin Zhou,Nikhil Kalasariya,Nengxu Li,Tao Wang,Jinxi Chen,Ling Kai Lee,Yuduan Wang,Jia Li,Martin Stolterfoht,Manling Sui,Yue Lu,Yi Hou","doi":"10.1038/s41563-025-02375-8","DOIUrl":null,"url":null,"abstract":"Efficient wide-bandgap perovskite solar cells have pushed tandem efficiencies to 34.9%, reinforcing their promise for next-generation photovoltaics. However, their commercial adoption is hindered by stability issues of wide-bandgap perovskites, especially under high-temperature maximum power point tracking conditions. Here we report the stabilization of ~1.7-eV wide-bandgap perovskites via intermediate phase evolution, enabling a self-guided crystal-growth mode. A CsI2Br intermediate phase forms during early stage deposition, directing the oriented growth of polycrystalline films with unique texturing. Atomic-scale scanning transmission electron microscopy reveals that the CsI2Br ( 1 2 ¯ 3 ) facet, with a 2.9-Å interplanar spacing, matches the perovskite (200) facet, guiding coherent {100} growth. This results in enhanced crystallinity, with a 2-order-magnitude increase in the (100) diffraction intensity and a reduced full-width at half-maximum from 0.249° to 0.148°, compared with solution-processed films. The resulting solar cells exhibit outstanding thermal and operational stability, maintaining performance under maximum power point tracking for over 3,000 h at room temperature and over 500 h at 110 °C, with a projected lifetime of ~70,000 h. With 21.37% power conversion efficiency and >84% fill factor, this work presents a compelling route towards stable, high-efficiency tandem photovoltaics.","PeriodicalId":19058,"journal":{"name":"Nature Materials","volume":"200 1","pages":""},"PeriodicalIF":38.5000,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Intermediate phase evolution for stable and oriented evaporated wide-bandgap perovskite solar cells.\",\"authors\":\"Zijing Dong,Jingcong Hu,Xiao Guo,Zhuojie Shi,Haijie Chen,Yunluo Wang,Ran Luo,Julian A Steele,Zachary Degnan,Eduardo Solano,Qilin Zhou,Nikhil Kalasariya,Nengxu Li,Tao Wang,Jinxi Chen,Ling Kai Lee,Yuduan Wang,Jia Li,Martin Stolterfoht,Manling Sui,Yue Lu,Yi Hou\",\"doi\":\"10.1038/s41563-025-02375-8\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Efficient wide-bandgap perovskite solar cells have pushed tandem efficiencies to 34.9%, reinforcing their promise for next-generation photovoltaics. However, their commercial adoption is hindered by stability issues of wide-bandgap perovskites, especially under high-temperature maximum power point tracking conditions. Here we report the stabilization of ~1.7-eV wide-bandgap perovskites via intermediate phase evolution, enabling a self-guided crystal-growth mode. A CsI2Br intermediate phase forms during early stage deposition, directing the oriented growth of polycrystalline films with unique texturing. Atomic-scale scanning transmission electron microscopy reveals that the CsI2Br ( 1 2 ¯ 3 ) facet, with a 2.9-Å interplanar spacing, matches the perovskite (200) facet, guiding coherent {100} growth. This results in enhanced crystallinity, with a 2-order-magnitude increase in the (100) diffraction intensity and a reduced full-width at half-maximum from 0.249° to 0.148°, compared with solution-processed films. The resulting solar cells exhibit outstanding thermal and operational stability, maintaining performance under maximum power point tracking for over 3,000 h at room temperature and over 500 h at 110 °C, with a projected lifetime of ~70,000 h. With 21.37% power conversion efficiency and >84% fill factor, this work presents a compelling route towards stable, high-efficiency tandem photovoltaics.\",\"PeriodicalId\":19058,\"journal\":{\"name\":\"Nature Materials\",\"volume\":\"200 1\",\"pages\":\"\"},\"PeriodicalIF\":38.5000,\"publicationDate\":\"2025-10-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nature Materials\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1038/s41563-025-02375-8\",\"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":"Nature Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1038/s41563-025-02375-8","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}
Intermediate phase evolution for stable and oriented evaporated wide-bandgap perovskite solar cells.
Efficient wide-bandgap perovskite solar cells have pushed tandem efficiencies to 34.9%, reinforcing their promise for next-generation photovoltaics. However, their commercial adoption is hindered by stability issues of wide-bandgap perovskites, especially under high-temperature maximum power point tracking conditions. Here we report the stabilization of ~1.7-eV wide-bandgap perovskites via intermediate phase evolution, enabling a self-guided crystal-growth mode. A CsI2Br intermediate phase forms during early stage deposition, directing the oriented growth of polycrystalline films with unique texturing. Atomic-scale scanning transmission electron microscopy reveals that the CsI2Br ( 1 2 ¯ 3 ) facet, with a 2.9-Å interplanar spacing, matches the perovskite (200) facet, guiding coherent {100} growth. This results in enhanced crystallinity, with a 2-order-magnitude increase in the (100) diffraction intensity and a reduced full-width at half-maximum from 0.249° to 0.148°, compared with solution-processed films. The resulting solar cells exhibit outstanding thermal and operational stability, maintaining performance under maximum power point tracking for over 3,000 h at room temperature and over 500 h at 110 °C, with a projected lifetime of ~70,000 h. With 21.37% power conversion efficiency and >84% fill factor, this work presents a compelling route towards stable, high-efficiency tandem photovoltaics.
期刊介绍:
Nature Materials is a monthly multi-disciplinary journal aimed at bringing together cutting-edge research across the entire spectrum of materials science and engineering. It covers all applied and fundamental aspects of the synthesis/processing, structure/composition, properties, and performance of materials. The journal recognizes that materials research has an increasing impact on classical disciplines such as physics, chemistry, and biology.
Additionally, Nature Materials provides a forum for the development of a common identity among materials scientists and encourages interdisciplinary collaboration. It takes an integrated and balanced approach to all areas of materials research, fostering the exchange of ideas between scientists involved in different disciplines.
Nature Materials is an invaluable resource for scientists in academia and industry who are active in discovering and developing materials and materials-related concepts. It offers engaging and informative papers of exceptional significance and quality, with the aim of influencing the development of society in the future.