David P. McMeekin, Philippe Holzhey, Sebastian O. Fürer, Steven P. Harvey, Laura T. Schelhas, James M. Ball, Suhas Mahesh, Seongrok Seo, Nicholas Hawkins, Jianfeng Lu, Michael B. Johnston, Joseph J. Berry, Udo Bach, Henry J. Snaith
{"title":"通过二甲基铵阳离子添加剂进行中间相工程,实现稳定的过氧化物太阳能电池","authors":"David P. McMeekin, Philippe Holzhey, Sebastian O. Fürer, Steven P. Harvey, Laura T. Schelhas, James M. Ball, Suhas Mahesh, Seongrok Seo, Nicholas Hawkins, Jianfeng Lu, Michael B. Johnston, Joseph J. Berry, Udo Bach, Henry J. Snaith","doi":"10.1038/s41563-022-01399-8","DOIUrl":null,"url":null,"abstract":"Achieving the long-term stability of perovskite solar cells is arguably the most important challenge required to enable widespread commercialization. Understanding the perovskite crystallization process and its direct impact on device stability is critical to achieving this goal. The commonly employed dimethyl-formamide/dimethyl-sulfoxide solvent preparation method results in a poor crystal quality and microstructure of the polycrystalline perovskite films. In this work, we introduce a high-temperature dimethyl-sulfoxide-free processing method that utilizes dimethylammonium chloride as an additive to control the perovskite intermediate precursor phases. By controlling the crystallization sequence, we tune the grain size, texturing, orientation (corner-up versus face-up) and crystallinity of the formamidinium (FA)/caesium (FA)yCs1–yPb(IxBr1–x)3 perovskite system. A population of encapsulated devices showed improved operational stability, with a median T80 lifetime (the time over which the device power conversion efficiency decreases to 80% of its initial value) for the steady-state power conversion efficiency of 1,190 hours, and a champion device showed a T80 of 1,410 hours, under simulated sunlight at 65 °C in air, under open-circuit conditions. This work highlights the importance of material quality in achieving the long-term operational stability of perovskite optoelectronic devices. The stability of halide perovskite solar cells, determined by film morphology, is paramount to their commercialization. Here, the authors introduce a high-temperature DMSO-free method that enables better control of the grain size, texturing, orientation and crystallinity to achieve improved device operational stability.","PeriodicalId":37,"journal":{"name":"Environmental Science & Technology Letters Environ.","volume":null,"pages":null},"PeriodicalIF":8.9000,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"26","resultStr":"{\"title\":\"Intermediate-phase engineering via dimethylammonium cation additive for stable perovskite solar cells\",\"authors\":\"David P. McMeekin, Philippe Holzhey, Sebastian O. Fürer, Steven P. Harvey, Laura T. Schelhas, James M. Ball, Suhas Mahesh, Seongrok Seo, Nicholas Hawkins, Jianfeng Lu, Michael B. Johnston, Joseph J. Berry, Udo Bach, Henry J. 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A population of encapsulated devices showed improved operational stability, with a median T80 lifetime (the time over which the device power conversion efficiency decreases to 80% of its initial value) for the steady-state power conversion efficiency of 1,190 hours, and a champion device showed a T80 of 1,410 hours, under simulated sunlight at 65 °C in air, under open-circuit conditions. This work highlights the importance of material quality in achieving the long-term operational stability of perovskite optoelectronic devices. The stability of halide perovskite solar cells, determined by film morphology, is paramount to their commercialization. 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Intermediate-phase engineering via dimethylammonium cation additive for stable perovskite solar cells
Achieving the long-term stability of perovskite solar cells is arguably the most important challenge required to enable widespread commercialization. Understanding the perovskite crystallization process and its direct impact on device stability is critical to achieving this goal. The commonly employed dimethyl-formamide/dimethyl-sulfoxide solvent preparation method results in a poor crystal quality and microstructure of the polycrystalline perovskite films. In this work, we introduce a high-temperature dimethyl-sulfoxide-free processing method that utilizes dimethylammonium chloride as an additive to control the perovskite intermediate precursor phases. By controlling the crystallization sequence, we tune the grain size, texturing, orientation (corner-up versus face-up) and crystallinity of the formamidinium (FA)/caesium (FA)yCs1–yPb(IxBr1–x)3 perovskite system. A population of encapsulated devices showed improved operational stability, with a median T80 lifetime (the time over which the device power conversion efficiency decreases to 80% of its initial value) for the steady-state power conversion efficiency of 1,190 hours, and a champion device showed a T80 of 1,410 hours, under simulated sunlight at 65 °C in air, under open-circuit conditions. This work highlights the importance of material quality in achieving the long-term operational stability of perovskite optoelectronic devices. The stability of halide perovskite solar cells, determined by film morphology, is paramount to their commercialization. Here, the authors introduce a high-temperature DMSO-free method that enables better control of the grain size, texturing, orientation and crystallinity to achieve improved device operational stability.
期刊介绍:
Environmental Science & Technology Letters serves as an international forum for brief communications on experimental or theoretical results of exceptional timeliness in all aspects of environmental science, both pure and applied. Published as soon as accepted, these communications are summarized in monthly issues. Additionally, the journal features short reviews on emerging topics in environmental science and technology.