Novel Fluorinated Dithienothiophene-Based Self-Assembled Monolayers as Hole-Selective Contacts for Mixed Tin–Lead Perovskite Solar Cells
Min Hsuan Tsai a
a Department of Chemical Engineering, National Chung Hsing University, Taichung, Taiwan
NIPHO26
Proceedings of International Conference on Perovskite Thin Film Photovoltaics and Perovskite Photonics and Optoelectronics (NIPHO26)
Pavia, Italy, 2026 June 8th - 9th
Organizers: Giulia Grancini, Feng Gao and Robert Hoye
Poster, Min Hsuan Tsai, 031
Publication date: 22nd April 2026

Mixed Tin-lead (Sn–Pb) perovskite are strong candidates for the narrow-bandgap sub-cell in all-perovskite tandems, but Sn²⁺ oxidation and poor buried-interface quality remain major obstacles.1 Conventional SAMs such as 2PACz and MeO-2PACz were not designed for the mixed Sn²⁺/Pb²⁺ surface, leaving a mismatch in both energy alignment and passivation.2 Here we introduce dithienothiophene (DTT)-based SAMs ’’ CHL-2, CHL-2-oF, and CHL-2-mF ’’carrying a fused DTT core, methoxytriphenylamine donors, and dual carboxylic acid anchors.3 DFT calculations show that fluorine at the meta-position makes the molecule a better match for the Sn²⁺/Pb²⁺ sites on the perovskite surface, and MD simulations confirm that CHL-2-mF binds more strongly to both the Sn–Pb perovskite and ITO than the other two SAMs.4 Films grown on fluorinated SAMs show larger crystalline domains and more uniform PL quenching across the active area.5 CHL-2-mF devices outperform both reference SAMs in VOC, fill factor, and PCE, with consistent results. These findings show that tuning the fluorine position on a DTT scaffold is an effective route to better buried interfaces in narrow-bandgap perovskite solar cells.

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