Abstract
Quasi-two-dimensional (2D) perovskites are notable for their diverse formulations and environmental stability. However, solution-processed quasi-2D perovskites often exhibit inherent multiple-quantum-well structures with broad phase distributions, limiting their efficiency in photovoltaic applications. Here, we demonstrate that incorporating rubidium ions effectively narrows the phase distribution in quasi-2D perovskite by accelerating the formation of the n = 1 2D perovskite phase during the initial crystallization stage. This leads to a decrease in the remaining free organic spacer cations, which in turn limits the transition to medium-n phases (n = 3, 4) and promotes the formation of high-quality 3D-like or large-n perovskites, ultimately enhancing charge transport of quasi-2D perovskite. Consequently, we achieve quasi-2D perovskite solar cells with a champion power conversion efficiency of 21.9%. Furthermore, the thermal stability of the unencapsulated devices containing rubidium is significantly improved, with the T80 lifetime under continuous 60 °C stress increasing from 1150 to over 3000 h.
| Original language | English |
|---|---|
| Pages (from-to) | 6064-6071 |
| Number of pages | 8 |
| Journal | ACS Energy Letters |
| Volume | 9 |
| Issue number | 12 |
| DOIs | |
| Publication status | Published - 13 Dec 2024 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
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