We report effects of an interface between
TiO2−perovskite and grain−grain boundaries of perovskite
films prepared by single step and sequential deposited
technique using different annealing times at optimum
temperature. Nanoscale kelvin probe force microscopy
(KPFM) measurement shows that charge transport in a
perovskite solar cell critically depends upon the annealing
conditions. The KPFM results of single step and sequential
deposited films show that the increase in potential barrier
suppresses the back-recombination between electrons in TiO2
and holes in perovskite. Spatial mapping of the surface
potential within perovskite film exhibits higher positive
potential at grain boundaries compared to the surface of the
grains. The average grain boundary potential of 300−400 mV is obtained upon annealing for sequentially deposited films. X-ray
diffraction (XRD) spectra indicate the formation of a PbI2 phase upon annealing which suppresses the recombination. Transient
analysis exhibits that the optimum device has higher carrier lifetime and short carrier transport time among all devices. An
optimum grain boundary potential and proper band alignment between the TiO2 electron transport layer (ETL) and the
perovskite absorber layer help to increase the overall device performance.