Recently, two-dimensional (2D)/three-dimensional (3D)
bilayer perovskite
solar cells (PSCs) show a great potential for commercialization due
to the combination of the fascinating photovoltaic performance of
3D perovskites and superior stability of 2D perovskites. However,
it is a challenge to nondestructively construct 2D/3D bilayer perovskites,
and the impact of the number of amine groups in ammonium spacer cations
on the properties of 2D/3D bilayer perovskites has not been investigated.
In this work, a novel interfacial post-treatment strategy is proposed
to nondestructively fabricate 2D/3D bilayer perovskite films using
the multi-ammonium molecule (MAM) vapor. Here, a series of MAMs with
three to six amine groups (3 to 6N), including diethylenetriamine
(DETA, 3N), triethylenetetramine (TETA, 4N), tetraethylenepentamine
(TEPA, 5N), and pentaethylenehexamine (PEHA, 6N), are applied and
compared. Benefiting from the strong interaction between MAMs and
perovskites, the MAM vapor post-treatment can in situ generate Dion–Jacobson (DJ) 2D capping layers on the surface
of 3D perovskite films. In comparison with the 3D perovskite film,
such DJ 2D/3D perovskite films exhibit improved film quality, effectively
passivated defects/traps, optimized interfacial band energy alignment,
and mitigatory tensile strain. In particular, the number of amine
groups in MAMs can dramatically influence the quality of DJ 2D/3D
bilayer perovskite films and their corresponding photovoltaic performance.
As the number of amine groups increases from DETA to PEHA, the efficiency
and stability of PSCs are boosted significantly. Consequently, the
PEHA-based DJ 2D/3D bilayer PSC delivers a champion power conversion
efficiency of 21.79% with a negligible hysteresis effect, elevated
reproducibility, and enhanced device stability. This work offers the
reference for designing novel and effective MAMs for nondestructively
fabricating high-performance 2D/3D bilayer PSCs.