Abstract

Two-dimensional (2D) Ruddlesden–Popper hybrid perovskites are a homologous series of compounds with the formula A′2An–1BnX3n+1 (A′ = bulky organic cation; A = small organic cation; B = Pb2+ or Sn2+, X = Cl–, Br–, I–; n is an integer) composed of inorganic octahedral layers separated by organic spacer cations. The octahedral layer thickness is modified by the stoichiometry of the A-site cation, but limited methods exist for controlled and discriminating synthesis for all compositions. We report a general synthesis method and its principles that yield phase-pure 2D hybrid perovskites; the chemistry operates within a dynamic equilibrium established by the molar solubility of the compounds within the homologous series. A solvent–antisolvent (HI–acetic acid) pair and the common-ion effect provide selective control over the molar solubility to precipitate phase-pure compounds, as is supported by simple and predictive calculations. Here, this approach is demonstrated in detail with A′ = n-butylammonium, A = meth...

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