We synthesize and characterize derivatives of the two-dimensional hybrid perovskite (2DHP) phenethylammonium lead iodide ((PEA)PbI) in which the para H on the cation is replaced with F, Cl, CH, or Br. These substitutions increase the length of the cation but leave the cross-sectional area unchanged, resulting in structurally similar PbI frameworks with increasing interlayer spacing. Longer cations result in broader, blue-shifted excitonic absorption spectra with reduced or eliminated structure, indicating greater energetic disorder. Photoluminescence spectra are largely invariant and insensitive to cation length, suggesting polaron formation stabilizes a structural and electronic minimum. Temperature-dependent line width analysis reveals excitons couple to a vibration on the organic framework that is weakly sensitive to these cation substitutions, and Raman spectra and electronic structure calculations support the presence of such a cationic mode. Despite carriers being confined to the inorganic framework, the length of the organic cation alters the optical and electronic properties of 2DHPs.
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