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Benign methylformamidinium byproduct induced by cation heterogeneity inhibits local formation of delta-phase perovskites
Efforts to enhance the efficiency and stability of formamidinium lead triiodide (FAPbI3) perovskite
solar cells (PSCs) have primarily focused on employing methylammonium chloride (MACl) as an
effective additive. MACl significantly improves the crystallinity and lowers the -to- phase transition
temperature of FAPbI3, thereby contributing to the remarkable efficiency of these solar cells. However,
upon evaporation with deprotonation of MACl during annealing, the highly reactive methylamine leads
to the formation of N-methylformamidinium (MFA+) cations. Despite their potential for significant
influence on the properties of FAPbI3 perovskites, the chemical and optoelectronic characteristics of
MFA+ in FAPbI3 remain poorly understood. This study investigates the unexplored role of MFA+ in
FAPbI3 perovskite with MACl incorporation through advanced nanoscale characterization techniques,
including photo-induced force microscopy (PiFM), four-dimensional scanning transmission electron
microscopy, and wavelength-dependent Kelvin probe force microscopy (KPFM). We reveal that MACl
induces compositional heterogeneities, particularly formamidinium (FA+) and MFA+ cation
inhomogeneities. Surprisingly, MACl selectively promotes the formation of MFAPbI3 at grain
boundaries (GBs) and as clusters near GBs. Additionally, we confirm that MFAPbI3 is a wide bandgap,
and charge carriers are effectively separated at GBs and clusters enriched with MFAPbI3. This is
particularly interesting because MFAPbI3, despite its crystal structural similarity to yellow phase δ-
FAPbI3, displays a high surface photovoltage, and does not deteriorate the solar cell performance. This
study not only provides insights into the byproduct formation of MFA+ induced by local cation
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heterogeneity after employing MACl, but also guides a crucial perspective for optimizing
formamidinium-based PSC design and performance