Density of States Broadening in CH 3 NH 3 PbI 3 Hybrid Perovskites Understood from ab initio Molecular Dynamics Simulations

Liujiang Zhou (1) , Amanda J Neukirch (1) , Dayton Vogel (2) , Dmitri Kilin (3) , Laurent Pedesseau (4) , Marcelo Carignano (5) , Aditya D Mohite (1) , Jacky Even (4) , Claudine Katan (6) , Sergei Tretiak (1)

1 LANL - Los Alamos National Laboratory
2 USD - University of South Dakota [Vermillion]
3 NDSU - North Dakota State University
4 FOTON - Institut des Fonctions Optiques pour les Technologies de l'informatiON
5 QEERI - Qatar Environment and Energy Research Institute
6 ISCR - Institut des Sciences Chimiques de Rennes

Lead-halide perovskites are the promising materials in optoelectronic devices for their unique properties including direct band gap, strong light absorption, high carrier mobility and low fabrication cost. Here, by using ab inito molecular dynamics and electronic structure calculations, we report a systematic study on the broadening density of states (DOS) deep in the valence bands that has been experimentally observed but absent in static calculations. We quantify the broadening DOS reduction from cubic phase to lower temperature tetragonal and orthorhombic phases and attribute observed effects to the molecular vibrations and the anharmonicity of iodine atoms motion. Specifically, the MA cations’ vibrations are strongly linked to the moderate C−N stretch and CH3 bend, as well as the strong CH3 and NH+ 3 stretches. These results present a theoretical perspective on the structural dynamics in lead halide perovskites which may be valuable for future studies toward desired functionalities in perovskite-based optoelectronic devices.

Domaines: Chimie; Physique [physics]

Liujiang Zhou, Amanda J Neukirch, Dayton Vogel, Dmitri Kilin, Laurent Pedesseau, et al.. Density of States Broadening in CH 3 NH 3 PbI 3 Hybrid Perovskites Understood from ab initio Molecular Dynamics Simulations. ACS Energy Letters, 2018, 3 (4), pp.787-793. ⟨10.1021/acsenergylett.8b00166⟩. ⟨hal-01724992⟩