SnO<sub>2</sub>/Perovskite Interface Engineering with Mixed-Halide Potassium Salts: A Pathway to Efficient and Stable Perovskite Solar Cells through a Combined Experimental-Density Functional Theory Approach

Tin(IV) oxide (SnO<sub>2</sub>) is a promising electron transport layer for n-i-p perovskite solar cells (PSCs) due to its high transmittance, excellent charge mobility, and strong chemical stability. However, surface defects such as oxygen vacancies and hydroxyl groups at the SnO<sub>2</sub>/perovskite interface degrade the device performance by increasing carrier recombination and accelerating degradation. While alkali halide salts offer a simple yet effective method for passivation, their enhancement mechanisms at the atomic level remain unclear, as most studies focus on bulk or surface effects rather than the heterointerface itself. Here, we introduce a potassium halide salt (PHS: KI, KCl, and KI+KCl) post-treatment to passivate the SnO<sub>2</sub>/MAPbI<sub>3</sub> interface. Our combined experimental and density functional theory (DFT) analyses demonstrate that K<sup>+</sup> and halide ions facilitate the removal of oxygen vacancies and extrinsic hydroxyl groups through the formation of KOH. This process effectively reduces the bond strength of surface hydroxyls and enhances interfacial ordering. This results in a smoother interface, larger perovskite grain sizes, improved adhesion, and enhanced charge extraction. The formation of Sn-Cl-Pb and Sn-I-Pb bonds, along with electrostatic interactions among interfacial K<sup>+</sup>, I<sup>-</sup> in the perovskite structure, and O<sup>2-</sup> in SnO<sub>2</sub>, strengthens the interface and reduces ion migration. KI-modified and mixed KI+KCl devices achieved power conversion efficiencies (PCEs) of 19.86% and 19.15%, respectively, outperforming untreated SnO<sub>2</sub>, which had a PCE of 18.41%. More importantly, the mixed KI+KCl treatment shows superior stability improvement compared to individual PHS treatments, retaining over 96% of the initial PCE after 1000 h under 40-50% relative humidity. These findings highlight the critical role of potassium salts in improving both efficiency and stability, offering an effective strategy for advancing PSC technology.

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Publication Details

Journal
ACS Applied Materials & Interfaces
Published
2025-05-14
DOI
https://doi.org/10.1021/acsami.5c04415
Citations
14
Primary Topic
Perovskite Materials and Applications
Type
article
Field-Weighted Citation Impact
10.23

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article

SnO2/Perovskite Interface Engineering with Mixed-Halide Potassium Salts: A Pathway to Efficient and Stable Perovskite Solar Cells through a Combined Experimental-Density Functional Theory Approach

Kay Thi Soe, Nopporn Rujisamphan, Ibrahim Muhammad Adam, Thidarat Supasai et al.
14 citations
ACS Applied Materials & Interfaces
Perovskite Materials and Applications
10.23
article

SnO2/Perovskite Interface Engineering with Mixed-Halide Potassium Salts: A Pathway to Efficient and Stable Perovskite Solar Cells through a Combined Experimental-Density Functional Theory Approach

Kay Thi Soe, Nopporn Rujisamphan, Ibrahim Muhammad Adam, Thidarat Supasai, Thana Sutthibutpong, Ekkaphop Ketsombun, Non Thongprong, Waranchit Ruengsrisang
article en
14 citations

Abstract

Tin(IV) oxide (SnO<sub>2</sub>) is a promising electron transport layer for n-i-p perovskite solar cells (PSCs) due to its high transmittance, excellent charge mobility, and strong chemical stability. However, surface defects such as oxygen vacancies and hydroxyl groups at the SnO<sub>2</sub>/perovskite interface degrade the device performance by increasing carrier recombination and accelerating degradation. While alkali halide salts offer a simple yet effective method for passivation, their enhancement mechanisms at the atomic level remain unclear, as most studies focus on bulk or surface effects rather than the heterointerface itself. Here, we introduce a potassium halide salt (PHS: KI, KCl, and KI+KCl) post-treatment to passivate the SnO<sub>2</sub>/MAPbI<sub>3</sub> interface. Our combined experimental and density functional theory (DFT) analyses demonstrate that K<sup>+</sup> and halide ions facilitate the removal of oxygen vacancies and extrinsic hydroxyl groups through the formation of KOH. This process effectively reduces the bond strength of surface hydroxyls and enhances interfacial ordering. This results in a smoother interface, larger perovskite grain sizes, improved adhesion, and enhanced charge extraction. The formation of Sn-Cl-Pb and Sn-I-Pb bonds, along with electrostatic interactions among interfacial K<sup>+</sup>, I<sup>-</sup> in the perovskite structure, and O<sup>2-</sup> in SnO<sub>2</sub>, strengthens the interface and reduces ion migration. KI-modified and mixed KI+KCl devices achieved power conversion efficiencies (PCEs) of 19.86% and 19.15%, respectively, outperforming untreated SnO<sub>2</sub>, which had a PCE of 18.41%. More importantly, the mixed KI+KCl treatment shows superior stability improvement compared to individual PHS treatments, retaining over 96% of the initial PCE after 1000 h under 40-50% relative humidity. These findings highlight the critical role of potassium salts in improving both efficiency and stability, offering an effective strategy for advancing PSC technology.

ACS Applied Materials & InterfacesVol. 17(21)
Kasetsart University (TH), Centre de Nanosciences et de Nanotechnologies (FR), King Mongkut's University of Technology Thonburi (TH)
National Research Council of Thailand, King Mongkut's University of Technology Thonburi
Openalex Percentile: Top 2%
Perovskite Materials and Applications
10.23
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