Anharmonicity Extends Carrier Lifetimes in Lead Halide Perovskites at Elevated Temperatures

Lead halide perovskites constitute a very promising class of materials for a broad range of solar and optoelectronic applications. Perovskites exhibit many unusual properties, and recent experiments demonstrate an unusual temperature dependence of charge carrier lifetimes. Focusing on the all-inorganic CsPbBr3, and using a combination of ab initio nonadiabatic molecular dynamics and time-domain density functional theory, we demonstrate that the unconventional behavior arises because of a highly anharmonic nature of atomic motions in perovskites. As temperature increases, perovskite structure undergoes a notable deformation, reflected in tilting of octahedral units, and experiences large-scale anharmonic movements away from the equilibrium geometry. As a result, the electronic energy gap increases, and phonon-induced loss of coherence within the electronic subsystem accelerates. These two factors slow down nonradiative electron-hole recombination, which constitutes the main limitation on efficiencies of perovskite solar, optical, and electronic devices. The increase of charge carrier lifetimes with temperature is particularly beneficial in applications, because materials heat up, for instance, from sunlight during solar energy harvesting. The behavior of the all-inorganic halide perovskite investigated here is different from that of hybrid organic-inorganic perovskites, which exhibit additional disorder associated with reorientations of the asymmetric organic cations. The reported simulations generate an in-depth understanding of the unusual properties of inorganic perovskites, relevant for photocatalytic, photovoltaic, electronic, and optical applications.