The surface passivation of metal oxide electron-transport
layers
(ETLs) is a powerful strategy for realizing high-performance perovskite
solar cells. The surface properties of ETLs strongly influence carrier
injection and transfer dynamics; therefore, control of the carrier
trap density is crucial. Semiconducting small molecules are considered
suitable materials for surface passivation. However, they are expensive
and vulnerable to humid atmospheres. Ultrathin polymer layers can
have poor surface coverage owing to their spinodal dewetting. In this
study, we employ adipoyl chloride as an organic ligand for the chemically
robust and efficient surface passivation of SnO2 ETLs.
Through the strong coordination of diacyl-metal cations, acyl groups
are adsorbed onto the SnO2 surfaces, and the density of
oxygen vacancies is significantly reduced. Furthermore, the changing
surface properties of the SnO2 ETLs also contribute to
the improvement of perovskite morphologies. The deeper energy levels
and reduced defect density of the ETLs promote electron injection
and transfer at the perovskite and ETL interface. The enlarged perovskite
grains are accompanied by improved electron mobility and reduced grain-boundary
density. The resulting power conversion efficiency (PCE) increases
from 19.36 to 21.41%. The normalized PCE is retained at 90.4% of the
initial value for 720 h under 1 sun illumination without the encapsulation
of the devices.