Enhanced coordination interaction with multi-site binding ligands for efficient and stable perovskite solar cells

增强与多位点结合配体的配位相互作用,可提高钙钛矿太阳能电池的效率和稳定性

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Abstract

Conventional passivating ligands bind to perovskite surfaces through only a single active site, which not only creates a resistive barrier due to dense ligand packing but also restricts the enhancement of device stability. Here, we identify an antimony chloride-N,N-dimethyl selenourea complex, Sb(SU)(2)Cl(3), as a multi-anchoring ligand to significantly enhance perovskite crystallinity, suppress defect formation, and dramatically improve moisture resistance and overall stability. As a result, we achieve a power conversion efficiency of 25.03% in fully air-processed perovskite solar cells fabricated using a two-step method-among the highest efficiencies reported for devices prepared under ambient conditions. Remarkably, unencapsulated cells exhibited linear extrapolated T(80) lifetimes of 23,325 h during dark shelf storage. Furthermore, these unencapsulated devices demonstrate exceptional thermal and operational stability, with T(80) lifetimes of 5,004 (at 85 °C) and 5,209 hours (under 1-sun illumination), respectively, ranking them among the most stable perovskite solar cells to date.

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