4.8 Article

Fluorine-Containing Passivation Layer via Surface Chelation for Inorganic Perovskite Solar Cells

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 62, Issue 6, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202216634

Keywords

Chelation; Defect Passivation; Inorganic; Perovskite; Solar Cells

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To improve the power conversion efficiency and stability of inorganic perovskite solar cells, a trifluoroacetamidine (TFA) passivator was designed to suppress film defects. TFA strongly chelates onto the perovskite surface to suppress iodide vacancy, and intermolecular hydrogen bonds form a robust shield against moisture. TFA-treated solar cells exhibited significantly suppressed recombination and achieved the highest record power conversion efficiencies for all-inorganic solar cells.
Minimizing surface defect is vital to further improve power conversion efficiency (PCE) and stability of inorganic perovskite solar cells (PSCs). Herein, we designed a passivator trifluoroacetamidine (TFA) to suppress CsPbI3-xBrx film defects. The amidine group of TFA can strongly chelate onto the perovskite surface to suppress the iodide vacancy, strengthened by additional hydrogen bonds. Moreover, three fluorine atoms allow strong intermolecular connection via intermolecular hydrogen bonds, thus constructing a robust shield against moisture. The TFA-treated PSCs exhibit remarkably suppressed recombination, yielding the record PCEs of 21.35 % and 17.21 % for 0.09 cm(2) and 1.0 cm(2) device areas, both of which are the highest for all-inorganic PSCs so far. The device also achieves a PCE of 39.78 % under indoor illumination, the highest for all-inorganic indoor photovoltaic devices. Furthermore, TFA greatly improves device ambient stability by preserving 93 % of the initial PCE after 960 h.

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