3D/1D Heterostructure Perovskite Engineering via 1D TMSPbI3 Templated Growth Toward Improved Efficiency and Moisture Stability in Solar Cellsopen access
- Authors
- Lima, Farihatun Jannat; Sandhu, Sanjay; Mensah, Appiagyei Ewusi; Rahman, Md. Mahbubur; Ahmed, Saif; Kaliamurthy, Ashok Kumar; Asiam, Francis Kwaku; Lee, Jae-Joon
- Issue Date
- Dec-2025
- Publisher
- Wiley-VCH GmbH
- Keywords
- 3D/1D heterostructures; aprotic sulfonium; hydrophobicity; perovskites; solar cells; stability
- Citation
- Solar RRL
- Indexed
- SCIE
SCOPUS
- Journal Title
- Solar RRL
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/62572
- DOI
- 10.1002/solr.202500865
- ISSN
- 2367-198X
2367-198X
- Abstract
- Perovskite solar cells (PSCs) combine high power conversion efficiency (PCE) with low fabrication cost, yet their instability under ambient conditions remains a major barrier to commercialization. The protic nature of conventional A-site cations renders perovskite films vulnerable to moisture-induced degradation. Here, we demonstrate a mixed-dimensional (3D/1D) compositional engineering strategy using an aprotic additive, trimethylsulfonium bromide (TMSBr), to enhance both the moisture stability and photovoltaic performance of PSCs. Incorporation of TMSBr into a ternary-cation perovskite precursor promotes the in situ formation of one-dimensional TMSPbI<inf>3</inf> during preannealing, which organizes preferentially along the grain boundaries to form a 3D/1D heterostructure. The hydrophobic 1D TMSPbI<inf>3</inf> effectively suppresses water penetration owing to the weak interaction between TMS+ and H<inf>2</inf>O molecules, resulting in improved film crystallinity and suppressed intergranular degradation. Devices based on this architecture achieve a high PCE of 21.65% and retain over 84% of their initial efficiency after 40 days of ambient exposure. These findings highlight aprotic sulfonium additives as a promising route toward intrinsically moisture-stable and durable perovskite photovoltaics. © 2025 Wiley-VCH GmbH.
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Collections - College of Engineering > Department of Energy and Materials Engineering > 1. Journal Articles

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