Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/156862
Title: Ammonium sulfate treatment at the TiO₂/perovskite interface boosts operational stability of perovskite solar cells
Authors: Bening Tirta Muhammad
Salim, Teddy
Bruno, Annalisa
Grimsdale, Andrew C.
Leong, Wei Lin
Keywords: Engineering::Materials::Energy materials
Issue Date: 2021
Source: Bening Tirta Muhammad, Salim, T., Bruno, A., Grimsdale, A. C. & Leong, W. L. (2021). Ammonium sulfate treatment at the TiO₂/perovskite interface boosts operational stability of perovskite solar cells. Journal of Materials Chemistry C, 9(40), 14334-14341. https://dx.doi.org/10.1039/D1TC02657G
Project: 2019-T2-2-106 
W1925d0106 
Journal: Journal of Materials Chemistry C
Abstract: Titanium dioxide (TiO2) electron transport layers (ETLs) are still widely used in perovskite solar cells (PSCs) due to their compatibility with existing printing technologies and favorable energy level alignment for efficient electron extraction. However, TiO2 ETLs suffer from surface defects, e.g. oxygen vacancies, that are detrimental to the perovskite/ETL interface stability, especially under operational conditions. Furthermore, hydroxyl groups present on the TiO2 surface also contribute to deprotonation of acidic organic cations in PSCs. We thus hypothesize that the metal oxide surface turns chemically reactive under 1-sun illumination whereby devices are highly populated with charge carriers and experience elevated temperatures (ca. 60 °C). Here, we introduced facile incorporation of sulfate species on the metal oxide surface to minimize chemical degradation at the perovskite/ETL interface. The sulfate treatment was found to minimally influence the perovskite film morphology grown on top of the ETLs, so ruling out morphological effects and allowing us to study the perovskite/ETL interface stability. We found that the sulfate treated devices exhibited enhanced operational stability under the initial maximum power point voltage (VMPP) over 1800 s of measurement. The sulfate treated devices retained 95% of their initial efficiency while the pristine devices already lost more than 40% of their initial efficiency. We also thermally aged encapsulated perovskite films coated on top of pristine and treated ETLs. We found that the thermally aged perovskite films coated on the pristine ETL contained perovskite hydrate species while the treated samples did not. We thus postulate that the water molecules contributing to hydrate formation were generated solely from the ETL/perovskite interface. Lastly, better energy alignment was also found between the perovskite and sulfate-treated ETL, which also contributes to the improved operational and thermal stability.
URI: https://hdl.handle.net/10356/156862
ISSN: 2050-7526
DOI: 10.1039/D1TC02657G
DOI (Related Dataset): 10.21979/N9/2CWHXO
Rights: © 2021 The Royal Society of Chemistry. All rights reserved. This paper was published in Journal of Materials Chemistry C and is made available with permission of The Royal Society of Chemistry.
Fulltext Permission: embargo_20220922
Fulltext Availability: With Fulltext
Appears in Collections:EEE Journal Articles
ERI@N Journal Articles
IGS Journal Articles
MSE Journal Articles

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