The tin oxide (SnO2) electron transport layer
(ETL)
plays a crucial role in perovskite solar cells (PSCs). However, the
heterogeneous dispersion of commercial SnO2 colloidal precursors
is far from optimized, resulting in dissatisfied device performance
with SnO2 ETL. Herein, a multifunctional modification material,
ammonium citrate (TAC), is used to modify the SnO2 ETL,
bringing four benefits: (1) due to the electrostatic interaction between
TAC molecules and SnO2 colloidal particles, more uniformly
dispersed colloidal particles are obtained; (2) the TAC molecules
distributed on the surface of SnO2 provide nucleation sites
for the perovskite film growth, promoting the vertical growth of the
perovskite crystal; (3) TAC-doped SnO2 shows higher electron
conductivity and better film quality than pristine SnO2 while offering better energy-level alignment with the perovskite
layer; and (4) TAC has functional groups of CO and N–H
containing lone pair electrons, which can passivate the defects on
the surface of SnO2 and perovskite films through chemical
bonding and inhibit the device hysteresis. In the end, the device
based on TAC-doped ETL achieved an increased power conversion efficiency
(PCE) of 21.58 from 19.75% of the reference without such treatment.
Meanwhile, the PSCs using the TAC-doped SnO2 as the ETL
maintained 88% of their initial PCE after being stored for about 1000
h under dark conditions and controlled RH of 10–25%.