TY - JOUR
T1 - Buried interface treatment using alkali metal hydroxides for efficient and durable perovskite solar cells
AU - Fujita, Yuki
AU - Koseki, Daichi
AU - Senba, Dai
AU - Purev-Ochir, Badamgarav
AU - Wu, Tianhao
AU - Raju, Telugu Bhim
AU - Senevirathne, Chathuranganie A.M.
AU - Wang, Pangpang
AU - Yamada, Sunao
AU - Song, Juntae
AU - Ida, Shintaro
AU - Guo, Zhanglin
AU - Matsusima, Toshinori
N1 - Publisher Copyright:
© 2025 International Solar Energy Society
PY - 2025/5/15
Y1 - 2025/5/15
N2 - The buried interface in perovskite solar cells (PSCs) is pivotal in influencing the quality of the perovskite films and the efficiency of charge extraction and transport. Recent studies have highlighted the potential of alkali metal ion-based materials for modifying this interface. In this work, we present the first systematic investigation of the effects of different alkali metal hydroxide treatments at the buried interface between the SnO2 electron transport layer and the perovskite light absorber layer. Our findings demonstrate that KOH treatment significantly enhances the power conversion efficiency (PCE), while CsOH treatment improves operational durability. To achieve a balance between efficiency and durability, we developed a dual alkali metal hydroxide treatment strategy. Notably, the sequence of hydroxide deposition was found to be critical. A KOH treatment followed by CsOH increased the efficiency of mixed cation-based PSCs from 18.46% to 20.31% and improved durability, allowing the device to retain 95% of its initial efficiency after 500 h of continuous illumination at room temperature. Furthermore, this dual treatment enhanced the PCE of formamidinium lead iodide-based PSCs from 21.31% to 21.68%, along with improved operational stability. This study introduces a straightforward yet highly effective method for buried interface modification, offering a versatile approach to simultaneously boost efficiency and durability in a wide range of PSC architectures.
AB - The buried interface in perovskite solar cells (PSCs) is pivotal in influencing the quality of the perovskite films and the efficiency of charge extraction and transport. Recent studies have highlighted the potential of alkali metal ion-based materials for modifying this interface. In this work, we present the first systematic investigation of the effects of different alkali metal hydroxide treatments at the buried interface between the SnO2 electron transport layer and the perovskite light absorber layer. Our findings demonstrate that KOH treatment significantly enhances the power conversion efficiency (PCE), while CsOH treatment improves operational durability. To achieve a balance between efficiency and durability, we developed a dual alkali metal hydroxide treatment strategy. Notably, the sequence of hydroxide deposition was found to be critical. A KOH treatment followed by CsOH increased the efficiency of mixed cation-based PSCs from 18.46% to 20.31% and improved durability, allowing the device to retain 95% of its initial efficiency after 500 h of continuous illumination at room temperature. Furthermore, this dual treatment enhanced the PCE of formamidinium lead iodide-based PSCs from 21.31% to 21.68%, along with improved operational stability. This study introduces a straightforward yet highly effective method for buried interface modification, offering a versatile approach to simultaneously boost efficiency and durability in a wide range of PSC architectures.
KW - Alkali metal hydroxide treatments
KW - Defect passivation
KW - Electron extraction
KW - Halide perovskites
KW - Solar cells
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U2 - 10.1016/j.solener.2025.113444
DO - 10.1016/j.solener.2025.113444
M3 - Article
AN - SCOPUS:105000605668
SN - 0038-092X
VL - 292
JO - Solar Energy
JF - Solar Energy
M1 - 113444
ER -