Abstract

Chemical passivation of defective perovskite surface is a fundamental strategy to stabilize solar cell operation by impeding the defect-dominant surface ion migration. Here, we show that the configuration of organic cations plays a key role in determining their surface adsorption energetics at various perovskite facets, which will strongly impact the spatial uniformity of the low-dimensional perovskite passivation layer (LDPL). A weak-anisotropic adsorption behavior is demonstrated for tertiary ammonium that can enable a conformal LDPL on the perovskite grain surface. Benefiting from comprehensive surface passivation, the migration of ionic perovskite species was suppressed and the as-fabricated p-i-n solar cells yielded an optimized power conversion efficiency of 22.6% with an expected T 80 lifetime of about 4,000 h under continuous 1-sun illumination. Our findings give insight into the design and preparation of heterostructured perovskite films toward efficient and stable solar cells. • Surface adsorption enthalpy of organic cations is closely related to their configuration • Tertiary ammonium passivation results in conformally capped low-dimension perov. phase • Ion migration is suppressed in heterostructured perovskite film • The as-modified solar cells possess a stable efficiency under various stressors Taking advantage of the weak-anisotropic adsorption nature of tertiary ammonium on perovskite facets, Zhou et al. demonstrate a comprehensive protection of perovskite grain surface by constructing a conformal low-dimensional perovskite passivation layer. The inhibited ion migration enables stabilized solar cell operation.

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