Solid-state
perovskite solar cells have been expeditiously developed
since the past few years. However, there are a number of open questions
and issues related to the perovskite devices, such as their long-term
ambient stability and hysteresis in current density–voltage
curves. We developed highly efficient and hysteresis-less perovskite
devices by changing the frequently used TiO
2
mesoscopic
layer with polymer-hybridized multidoped ZnO nanocrystals in a common
n–i–p structure for the first time. The gradual adjustment
of ZnO conduction band position using single- and multidopant atoms
will likely enhance the power conversion efficiency (PCE) from 8.26
to 13.54%, with PCE
max
= 15.09%. The highest PCE
avg
of 13.54% was demonstrated by 2 atom % boron and 6 atom % fluorine
co-doped (B, F:ZnO) nanolayers (using optimized film thickness of
160 nm) owing to their highest conductivity, carrier concentration,
optical transmittance, and band-gap energy compared to other doped
films. We also successfully apply a fine polyethylenimine thin layer
on the doped ZnO nanolayers, causing the reduction in work function
and overall demonstrating the enhancement in PCE from ∼10.86%
up to 16.20%. A polymer-mixed electron-transporting layer demonstrates
the remarkable PCE
max
of 20.74% by decreasing the trap
sites in the oxide layer that probably reduces the chances of carrier
interfacial recombination originated from traps and thus improves
the device performance. Particularly, we produce these electron-rich
multidoped ZnO nanolayers via electrospray technique, which is highly
suitable for the future development of perovskite solar cells.