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Redirecting wet-interfacial redox pathways for efficient inverted perovskite solar cells.

Created on 21 Aug 2026

Authors

Zheng Liang, Boyuan Liu, Yuelong Li, Yalan Zhang, Yi Yang, Shengbin Cheng, Linchuan Ma, Bao Tu, Hua-Chao Liu, Huifen Xu, Yuqi Bao, Minghui Fan, Peide Zhu, Xianfu Zhang, Congqi Li, Hui Zhang, Xinyuan Zhang, Yuheng Li, Guodong Chen, Cheng Liu, Chen Zhu, Chuying Ouyang, Nam-Gyu Park, Yong Zhang

Published in

Science (New York, N.Y.). Volume 393. Issue 6813. Pages 800-806. Aug 20, 2026. Epub Aug 20, 2026.

Abstract

Carbazole-based phosphonic acid self-assembled monolayers (SAMs) are essential for high-efficiency p-i-n perovskite solar cells. However, during processing, these SAMs inevitably contact perovskite inks, where their acidity triggers a dimethyl sulfoxide (DMSO)-mediated iodide redox reaction that imprints device performance, representing a universal bottleneck for inverted devices. We resolve this SAM-triggered redox mechanism and introduce chemistry-matched hydrazide additives to mitigate the degradation. These additives abrogate DMSO activation and redirect unwanted by-products toward benign hydrazide-formamidinium adducts. Consequently, we achieved power conversion efficiencies (PCEs) of 27.7% (certified 27.4%) in small-area (0.06 cm2) cells and 20.1% in 2.0 m2 modules, along with T95 lifetimes of ~2000 hours of maximum power point tracking (MPPT) at 85°C and ~1500 hours MPPT at 85°C and 85% relative humidity.

PMID:
42623478
Bibliographic data and abstract were imported from PubMed on 21 Aug 2026.

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