{"title":"利用螯合配体进行界面配位,实现运行稳定的过氧化物太阳能模块","authors":"Bingkun Tian, Peikun Zhang, Tianjun Liu, Weicun Chu, Yuyang Long, Peng Xu, Ying Jiang, Jinping Zhang, Yajing Tang, Xiangnan Sun, Riming Nie, Xiaoming Zhao, Wanlin Guo, Zhuhua Zhang","doi":"10.1039/d4ee02803a","DOIUrl":null,"url":null,"abstract":"Perovskite solar cells (PSCs) feature a higher maximum theoretical efficiency and a lower cost than silicon-based solar cells, while also offering additional advantages of being flexible and transparent. However, the commercialization of PSCs remains a great challenge due to rapidly degraded efficiency and stability when scaled up to industrial sizes. Here, we develop an interfacial coordination strategy utilizing chelating ligands to address both the efficiency and stability issues on large scale. The ligands can form a layer of Pb (II) coordination polymers with robust chemical bonds that not only effectively passivate surface defects but also serve as a tightly adhered capping layer for protecting the perovskite surfaces. Then, the as-fabricated solar module with an area of up to 31.6 cm2 exhibits a projected T80 lifetime of over 9,000 hours under 1-sun illumination at 25 °C. Moreover, the ligands introduce suitable energy levels between the perovskite and electron charge transport layer to facilitate charge transfer across the interface. As a result, we simultaneously achieve a power conversion efficiency of 25.0% for a 0.16 cm2 single cell, and 22.6% for a 31.6 cm2 module, comparable to the efficiencies achieved by state-of-the-art solar modules of similar sizes.","PeriodicalId":72,"journal":{"name":"Energy & Environmental Science","volume":"245 1","pages":""},"PeriodicalIF":32.4000,"publicationDate":"2024-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Interfacial coordination utilizing chelating ligands for operationally stable perovskite solar modules\",\"authors\":\"Bingkun Tian, Peikun Zhang, Tianjun Liu, Weicun Chu, Yuyang Long, Peng Xu, Ying Jiang, Jinping Zhang, Yajing Tang, Xiangnan Sun, Riming Nie, Xiaoming Zhao, Wanlin Guo, Zhuhua Zhang\",\"doi\":\"10.1039/d4ee02803a\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Perovskite solar cells (PSCs) feature a higher maximum theoretical efficiency and a lower cost than silicon-based solar cells, while also offering additional advantages of being flexible and transparent. However, the commercialization of PSCs remains a great challenge due to rapidly degraded efficiency and stability when scaled up to industrial sizes. Here, we develop an interfacial coordination strategy utilizing chelating ligands to address both the efficiency and stability issues on large scale. The ligands can form a layer of Pb (II) coordination polymers with robust chemical bonds that not only effectively passivate surface defects but also serve as a tightly adhered capping layer for protecting the perovskite surfaces. Then, the as-fabricated solar module with an area of up to 31.6 cm2 exhibits a projected T80 lifetime of over 9,000 hours under 1-sun illumination at 25 °C. Moreover, the ligands introduce suitable energy levels between the perovskite and electron charge transport layer to facilitate charge transfer across the interface. As a result, we simultaneously achieve a power conversion efficiency of 25.0% for a 0.16 cm2 single cell, and 22.6% for a 31.6 cm2 module, comparable to the efficiencies achieved by state-of-the-art solar modules of similar sizes.\",\"PeriodicalId\":72,\"journal\":{\"name\":\"Energy & Environmental Science\",\"volume\":\"245 1\",\"pages\":\"\"},\"PeriodicalIF\":32.4000,\"publicationDate\":\"2024-11-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Energy & Environmental Science\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1039/d4ee02803a\",\"RegionNum\":1,\"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":"Energy & Environmental Science","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1039/d4ee02803a","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Interfacial coordination utilizing chelating ligands for operationally stable perovskite solar modules
Perovskite solar cells (PSCs) feature a higher maximum theoretical efficiency and a lower cost than silicon-based solar cells, while also offering additional advantages of being flexible and transparent. However, the commercialization of PSCs remains a great challenge due to rapidly degraded efficiency and stability when scaled up to industrial sizes. Here, we develop an interfacial coordination strategy utilizing chelating ligands to address both the efficiency and stability issues on large scale. The ligands can form a layer of Pb (II) coordination polymers with robust chemical bonds that not only effectively passivate surface defects but also serve as a tightly adhered capping layer for protecting the perovskite surfaces. Then, the as-fabricated solar module with an area of up to 31.6 cm2 exhibits a projected T80 lifetime of over 9,000 hours under 1-sun illumination at 25 °C. Moreover, the ligands introduce suitable energy levels between the perovskite and electron charge transport layer to facilitate charge transfer across the interface. As a result, we simultaneously achieve a power conversion efficiency of 25.0% for a 0.16 cm2 single cell, and 22.6% for a 31.6 cm2 module, comparable to the efficiencies achieved by state-of-the-art solar modules of similar sizes.
期刊介绍:
Energy & Environmental Science, a peer-reviewed scientific journal, publishes original research and review articles covering interdisciplinary topics in the (bio)chemical and (bio)physical sciences, as well as chemical engineering disciplines. Published monthly by the Royal Society of Chemistry (RSC), a not-for-profit publisher, Energy & Environmental Science is recognized as a leading journal. It boasts an impressive impact factor of 8.500 as of 2009, ranking 8th among 140 journals in the category "Chemistry, Multidisciplinary," second among 71 journals in "Energy & Fuels," second among 128 journals in "Engineering, Chemical," and first among 181 scientific journals in "Environmental Sciences."
Energy & Environmental Science publishes various types of articles, including Research Papers (original scientific work), Review Articles, Perspectives, and Minireviews (feature review-type articles of broad interest), Communications (original scientific work of an urgent nature), Opinions (personal, often speculative viewpoints or hypotheses on current topics), and Analysis Articles (in-depth examination of energy-related issues).