Triple-cation perovskite solar cells fabricated by a hybrid PVD/blade coating process using green solvents

The scalability of highly efficient organic-inorganic perovskite solar cells (PSCs) is one of the major challenges of solar module manufacturing. Various scalable methods have been explored to strive for uniform perovskite films of high crystal quality on large-area substrates, but each of these met...

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Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2021-12, Vol.9 (47), p.2668-26687
Hauptverfasser: Siegrist, Severin, Yang, Shih-Chi, Gilshtein, Evgeniia, Sun, Xiaoxiao, Tiwari, Ayodhya N, Fu, Fan
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Sprache:eng
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Zusammenfassung:The scalability of highly efficient organic-inorganic perovskite solar cells (PSCs) is one of the major challenges of solar module manufacturing. Various scalable methods have been explored to strive for uniform perovskite films of high crystal quality on large-area substrates, but each of these methods has individual limitations on the potential of successful commercialization of perovskite photovoltaics. Here, we report a fully scalable hybrid process, which combines vapor- and solution-based techniques to deposit high quality uniform perovskite films on large-area substrates. This two-step process does not use toxic solvents, and it further allows easy implementation of passivation strategies and additives. We fabricate PSCs based on this process and use blade coating to deposit a SnO 2 electron transporting layer and Spiro-OMeTAD hole transporting layer without halogenated solvents in ambient air. The fabricated PSCs have achieved open-circuit voltage up to 1.16 V and power conversion efficiency of 18.7% with good uniformity on 5 cm × 5 cm substrates. A novel and scalable PVD/blade coating method of the perovskite absorber is presented. In conjunction with charge transporting layers blade coated in ambient air using non-toxic solvents, these perovskite solar cells achieved 18.7% efficiency.
ISSN:2050-7488
2050-7496
DOI:10.1039/d1ta07579a