Quantum-confined two-dimensional (2D) Ruddlesden–Popper
(RP) perovskite nanoplates (NPls) are drawing considerable attention
in recent times. The effect of external perturbations like air, moisture,
heat, polarity of the solvent, and, specifically, light irradiation
has significant impact on the RP perovskite structure in different
ways. Though some reports are available on the effect of light irradiation
on RP NPl single crystals, films, and flakes, no comprehensive study
is available for the RP NPl colloidal state. To extend the understanding,
we studied the fate of UV irradiation on a colloidal, orange-emitting
oleylammonium iodide-based RP NPl, (C18H35NH3)2(CH3NH3PbI3)2PbI4 (n = 3). A constant UV exposure
for 10 h transforms the RP NPl structure into a purely 3D methylammonium
lead iodide (CH3NH3PbI3, MAPbI3) nanorod (NR) having a photoluminescence quantum yield of
65%. Our experimental results reveal that this structural transformation
takes place by ligand desorption, followed by structural association
in an oriented fashion. The obtained MAPbI3 NR shows excellent
optical and crystalline phase stability for more than 2 months.