Abstract
The advancement of wide-bandgap (WBG) Sn-perovskite devices is
substantially hindered by seasonal instability and limited
reproducibility, primarily due to moisture-induced over-doping of
PEDOT:PSS and Sn2+ oxidation. Here, we introduce a
hydrophobic proton-locking interface engineering strategy by
incorporating a novel S-benzyl-L-cysteine (SBLC) molecule into
PEDOT:PSS. The hydrophobic benzyl backbone, amine groups, and
significant dipole moment of SBLC facilitate strong coordination with Sn2+,
effectively preventing moisture ingress and stabilizing buried
interfacial energetics. This multifunctional modulation suppresses
defects and promotes uniform crystallization across varying humidity and
seasonal conditions. The optimized Target device, based on a WBG
Sn-perovskite composition of PEA0.10FA0.75EA0.15SnI2.15Br0.85,
achieves a power conversion efficiency of 11.50% and retains >80% of
its average performance across 279 devices fabricated monthly over 11
months, thereby establishing the first seasonal reproducibility
benchmark. Furthermore, this approach exhibits increased stability of
various stress conditions and enables a record efficiency of 17.40% in
all-perovskite tandem devices featuring a WBG Sn-perovskite. These
findings provide a scalable pathway toward reproducible,
tandem-compatible, lead-free photovoltaics.
| Original language | English |
|---|---|
| Article number | e05598 |
| Pages (from-to) | 1-13 |
| Number of pages | 13 |
| Journal | Advanced Energy Materials |
| Volume | 16 |
| Issue number | 9 |
| Early online date | 26 Dec 2025 |
| DOIs | |
| Publication status | Published - 4 Mar 2026 |
Keywords
- interface engineering
- proton-locking
- seasonal reproducibility
- tin-based perovskite
- wide-bandgap
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