Buried Interface Modification Using Diammonium Ligand Enhances Mechanical Durability of Flexible Perovskite Solar Cells

Flexible perovskite solar cells (F-PSCs) hold great potential for lightweight photovoltaic applications due to their flexibility, bending compatibility, and low manufacturing cost. However, tin oxide (SnO2), as a common electron transport layer (ETL) used in F-PSCs, typically suffers from high-density surface defects that hinder the charge extraction efficiency and deteriorate the crystallization quality of the upper perovskite film. Additionally, the poor buried interface quality intensifies lattice extrusion and strain residue across the perovskite films, further aggravating the mechanical brittleness in devices. To address the issues, we developed a molecular bridging strategy by introducing the 2,2′-oxybis(ethylenediamine) dihydrochloride (DO) at the perovskite/SnO2 interface. The diammonium groups of spacer ligands can achieve the bidentate anchoring on the SnO2 and perovskite films, cooperating with the oxygen atom on the alkyl chain to passivate the charged defects at the buried interface. The tailored interface properties also endow the optimized crystallization quality of perovskite films and significantly alleviate tensile strain to strengthen the perovskite’s pliability. As a result, the F-PSCs achieved a champion efficiency of 23.50%, outperforming the value of 21.87% for the control device. Furthermore, the devices exhibited excellent mechanical robustness, maintaining 90% of the initial PCE after 6000 bending cycles at a radius of 4 mm. This work presents a reliable strategy for the synergistic optimization of the buried contact at the electron extraction interface, contributing to the further development of efficient and stable F-PSCs.