Abstract
Suppressing the defects from SnO2 and perovskite interface is essential for the fabrication of large-area n–i–p perovskite solar cells (PSCs) with the needed lifetime and efficiency for commercialization. Here, we report the employment of l-citrulline (CIT), which has amino acid (─COOH, ─NH2) and urea (─NH─CO─NH2) groups, during SnO2 colloidal dispersion to function as a molecular bridge to modulate the SnO2/perovskite buried interface. The amino acid group can effectively coordinate with Sn4+ to passivate the oxygen vacancy defects of SnO2, and the urea group can interact with uncoordinated Pb2+ and I−. These interactions not only improve the electron mobility of SnO2 but also facilitate the formation of larger grain-size perovskite film. In addition, they can also inhibit the generation of excess PbI2 and the nonphotoactive δ phase to result in suppressed trap-assisted nonradiative recombination. Consequently, the incorporation of CIT helps achieve a champion power conversion efficiency (PCE) of 25.95% (0.07065 cm2) in PSC with improved shelf life/light soaking stability. When combined with an antisolvent-free slot-die coating technique in air, the solar modules (23.26 cm2) could achieve a PCE of 22.70%, which is among the highest PCE reported so far.
| Original language | English |
|---|---|
| Article number | e202508169 |
| Journal | Angewandte Chemie - International Edition |
| Volume | 64 |
| Issue number | 30 |
| DOIs | |
| State | Published - 21 Jul 2025 |
Keywords
- Buried interface
- Long-term stability
- Molecular bridge linker
- Perovskite solar cells
- Solar modules
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