Self-Healing Beyond Molecular Iodine Locking in Formamidinium Lead Triiodide Perovskites

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Authors: Liangyu Zhao, Yi Chi, Zijin Wu, Jaewang Park, Junsu Kim, Yue Qiang, Huaiman Cao, Shouye Dai, Yulong Chen, Geert Brocks, Licheng Sun, Sang Il Seok
+2 more Shuxia Tao, Ze Yu
Cited by: 1
References: 47

Abstract

Iodide-based perovskites commonly undergo irreversible decomposition under operational conditions due to molecular iodine (I 2 ) generation, severely impacting device longevity. In this study, we introduce 1,4-dithiane (DT) as an efficient molecular iodine locking (MIL) agent at grain boundaries and surfaces of formamidinium lead triiodide (FAPbI 3 ) perovskite absorbers. The incorporation of DT not only minimizes iodine evaporation through robust S···I halogen bonding but also facilitates the dissociation of I–I bonds, enabling dynamic self-healing of the δ-phase into the photoactive α-phase of FAPbI 3 at room temperature. This “self-healing beyond MIL” mechanism ensures exceptional device stability under continuous light soaking (ISOS-L-1I), light–dark cycling (ISOS-LC-1I), and damp-heat stress (ISOS-D-3), with PSCs retaining >95% of their initial performance for 1000 h. The established iodine cycling process─comprising iodine capture, iodide regeneration, and vacancy backfilling─substantially enhances perovskite durability. Overall, this strategy presents a promising pathway for advancing robust PSCs and other iodine-sensitive optoelectronic devices.

Fields of Study & Subjects

Perovskite Materials and Applications Layered Double Hydroxides Synthesis and Applications Covalent Organic Framework Applications

Publication details

Journal / source
ACS Energy Letters
Publisher
American Chemical Society (ACS)
Volume
11
Issue
3
Pages
2959–2966
Publication date
13 February 2026
Language
EN