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A critical limitation of formamidinium lead iodide (FAPbI 3 ) perovskite solar cells (PSCs) lies in the intrinsic instability of the ionic–covalent Pb–I octahedral lattice, relative to the unfavorable hexagonal δ-phase under operating conditions. We report an entropy-regulating molecular-lock strategy using 1-pyridin-3-ylmethyl-piperazine hydrochloride (3-PMPCl). Strong interactions between the perovskite lattice surface and 3-PMPCl modulate the rotational freedom of organic cations and suppress the detrimental entropy increase associated with PbI 6 4− octahedra disorder or expansion. This entropy-favored environment intrinsically increases the phase transition energy barrier. The uniform distribution and strong adsorption of 3-PMPCl stabilize the α-phase under elevated temperature and humidity conditions. We achieved a certified power conversion efficiency (PCE) of 27.6% in FAPbI 3 -based PSCs. However, the operational stability of such champion devices remains below the state of the art. Adopting a stable bismuth electrode addresses this issue with a slight reduction in efficiency, yielding a device that retains 93.0% of its initial PCE (26.8%) after 1011 hours at 85°C under 1-sun illumination.
Miao et al. (Thu,) studied this question.
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