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Sustainable Stabilization of Perovskite Solar Cells Using Multifunctional Ammonium Alginate for over 26% Efficiency

Jianting HuangFujian Provincial Key Laboratory of Electrochemical Energy Storage Materials Fuzhou University Fuzhou Fujian ChinaManzhen FangFujian Provincial Key Laboratory of Electrochemical Energy Storage Materials Fuzhou University Fuzhou Fujian ChinaPenglin CaiFujian Provincial Key Laboratory of Electrochemical Energy Storage Materials Fuzhou University Fuzhou Fujian ChinaSongting LiFujian Provincial Key Laboratory of Electrochemical Energy Storage Materials Fuzhou University Fuzhou Fujian ChinaSenhu LiuFujian Provincial Key Laboratory of Electrochemical Energy Storage Materials Fuzhou University Fuzhou Fujian ChinaIlhom TojiboyevInstitute of Ion Plasma Laser TechnologiesMingdeng WeiFujian Provincial Key Laboratory of Electrochemical Energy Storage Materials Fuzhou University Fuzhou Fujian ChinaJingwei ZhuFujian Provincial Key Laboratory of Electrochemical Energy Storage Materials Fuzhou University Fuzhou Fujian ChinaYafeng LiFujian Provincial Key Laboratory of Electrochemical Energy Storage Materials Fuzhou University Fuzhou Fujian China
2026en
ABI

Abstract

ABSTRACT Metal halide perovskite solar cells have emerged as a revolutionary photovoltaic technology due to their exceptional optoelectronic properties and low‐cost fabrication processes. However, the commercialization is significantly hindered by insufficient operational stability. The inherent ionic character of the perovskite lattice renders it susceptible to degradation under thermal and environmental stresses, primarily initiated by the loss of volatile organic cations and ion migration. Although defect passivation strategies have been extensively explored, a solution that effectively addresses the thermodynamic instability of the organic cation lattice site remains highly desirable. Herein, we first introduced ammonium alginate, a benign biopolymer, as a multifunctional stabilizer, which are proposed to suppress the deprotonation of formamidinium cations, thereby anchoring the A‐site, while the carboxylate groups can efficiently passivate undercoordinated Pb 2+ ions, reducing defect states. The synergistic effect, combined with the induced preferential crystallographic orientation and suppressed ion migration, significantly enhanced the device's photovoltaic performance‐increasing the power conversion efficiency from 24.05% to 26.12%, with the fill factor improved from 80.2% to 85.1%. Meanwhile, the devices have also exhibited an exceptional thermal and ambient stability, retaining over 80% of their initial efficiency under accelerated thermal aging and ambient exposure.

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