Conjugated anion modulation for extended defect passivation at buried interfaces in perovskite solar cells

Defect-rich buried interfaces remain a critical bottleneck limiting the efficiency and stability of perovskite solar cells (PSCs). Notably, oxygen vacancies at the SnO 2 /perovskite interface act as dominant nonradiative recombination centers, severely inhibiting device performance. While conventional interfacial passivation strategies have primarily focused on localized coordination by anionic anchoring groups, the role of π-conjugated anions in interfacial modifiers remains insufficiently understood. Here, a conjugated anion modulation is established by comparing potassium acetate (KAc) and potassium sorbate (KSb), which share identical K + –carboxylate frameworks but differ in anion conjugation, elucidating the contribution of the π-conjugation effect in interfacial defect suppression. Unlike the localized interaction of KAc, the π-conjugated framework of KSb enables more delocalized electronic interactions, contributing to spatially extended passivation from the buried interface into the perovskite region. These extended interactions enable favorable energy-level alignment and effective passivation of oxygen vacancies in SnO 2 , while also improving perovskite crystallinity and suppressing interfacial recombination. As a result, KSb-modified devices achieve an efficiency of 22.16% with an open-circuit voltage of 1.183 V and a fill factor of 84.30%, surpassing KAc and control devices. Unencapsulated KSb devices retain 97% of their initial efficiency after 1000 h under dark ambient storage and demonstrate improved film-level thermal stability. Our findings highlight π-conjugated anion engineering as an effective strategy for achieving spatially extended defect passivation at buried interfaces, offering potential for molecular design for improving perovskite optoelectronic devices. Introducing a π-conjugated anion at the SnO 2 /perovskite interface enables extended interfacial passivation, optimized energy-level alignment, and improved crystallization and charge extraction in buried SnO 2 /perovskite interfaces

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Publication Details

Journal
Advanced Composites and Hybrid Materials
Published
2026-07-21
DOI
https://doi.org/10.1007/s42114-026-01958-6
Primary Topic
Perovskite Materials and Applications
Type
article
Field-Weighted Citation Impact
0.00

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article

Conjugated anion modulation for extended defect passivation at buried interfaces in perovskite solar cells

J W Park, Soo Young Kim, Won Jin Jang, Hyeon Kim et al.
Advanced Composites and Hybrid Materials
Perovskite Materials and Applications
article

Conjugated anion modulation for extended defect passivation at buried interfaces in perovskite solar cells

J W Park, Soo Young Kim, Won Jin Jang, Hyeon Kim, Donghwa Lee
article en

Abstract

Defect-rich buried interfaces remain a critical bottleneck limiting the efficiency and stability of perovskite solar cells (PSCs). Notably, oxygen vacancies at the SnO 2 /perovskite interface act as dominant nonradiative recombination centers, severely inhibiting device performance. While conventional interfacial passivation strategies have primarily focused on localized coordination by anionic anchoring groups, the role of π-conjugated anions in interfacial modifiers remains insufficiently understood. Here, a conjugated anion modulation is established by comparing potassium acetate (KAc) and potassium sorbate (KSb), which share identical K + –carboxylate frameworks but differ in anion conjugation, elucidating the contribution of the π-conjugation effect in interfacial defect suppression. Unlike the localized interaction of KAc, the π-conjugated framework of KSb enables more delocalized electronic interactions, contributing to spatially extended passivation from the buried interface into the perovskite region. These extended interactions enable favorable energy-level alignment and effective passivation of oxygen vacancies in SnO 2 , while also improving perovskite crystallinity and suppressing interfacial recombination. As a result, KSb-modified devices achieve an efficiency of 22.16% with an open-circuit voltage of 1.183 V and a fill factor of 84.30%, surpassing KAc and control devices. Unencapsulated KSb devices retain 97% of their initial efficiency after 1000 h under dark ambient storage and demonstrate improved film-level thermal stability. Our findings highlight π-conjugated anion engineering as an effective strategy for achieving spatially extended defect passivation at buried interfaces, offering potential for molecular design for improving perovskite optoelectronic devices. Introducing a π-conjugated anion at the SnO 2 /perovskite interface enables extended interfacial passivation, optimized energy-level alignment, and improved crystallization and charge extraction in buried SnO 2 /perovskite interfaces

Advanced Composites and Hybrid Materials
Pohang University of Science and Technology (KR), Korea University (KR)
National Research Foundation of Korea
Affordable and clean energy
Openalex Percentile: Top 15%
Perovskite Materials and Applications
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