Tin dioxide (SnO2), in perovskite solar cells (PSCs),
stands out as the material most suited to the electron transport layer
(ETL), yielding advantages with regard to ease of preparation, high
mobility, and favorable energy level alignment. Nonetheless, there
is a chance that energy losses from defects in the SnO2 and interface will result in a reduction in the V
oc. Consequently, optimizing the interfaces within solar
cell devices is a key to augmenting both the efficiency and the stability
of PSCs. Herein this present study, we introduced butylammonium chloride
(BACl) into the SnO2 ETL. The resulting optimized SnO2 film mitigated interface defect density, thereby improving
charge extraction. The robust bonding capability of negatively charged
Cl– ions facilitated their binding with noncoordinated
Sn4+ ions, effectively passivating defects associated with
oxygen vacancies and enhancing charge transport within the SnO2 ETL. Concurrently, doped BA+ and Cl– diffused into the perovskite lattice, fostering perovskite grain
growth and reducing the defects in perovskite. In comparison to the
control device, the V
oc saw a 70 mV increase,
achieving a champion efficiency of 22.86%. Additionally, following
1000 h of ambient storage, the unencapsulated device based on SnO2 preburied with BACl retained around 90% of its initial photovoltaic
conversion efficiency.