Thermodynamic Origin of the Photostability of the Two-Dimensional Perovskite PEA<sub>2</sub>Pb(I<sub>1–<i>x</i></sub>Br<sub><i>x</i></sub>)<sub>4</sub>
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The two-dimensional (2D) mixed halide perovskite PEA2Pb(I1–xBrx)4 exhibits high phase stability under illumination as compared to the three-dimensional (3D) counterpart MAPb(I1–xBrx)3. We explain this difference using a thermodynamic theory that considers the sum of a compositional and a photocarrier free energy. Ab initio calculations show that the improved compositional phase stability of the 2D perovskite is caused by a preferred I–Br distribution, leading to a much lower critical temperature for halide segregation in the dark than for the 3D perovskite. Moreover, a smaller increase of the band gap with Br concentration x and a markedly shorter photocarrier lifetime in the 2D perovskite reduce the driving force for phase segregation under illumination, enhancing the photostability.
