Shallow trapping vs. deep polarons in a hybrid lead halide perovskite, CH3NH3PbI3. Issue 40 (22nd August 2017)

• Record Type: Journal Article
• Authors: Kang, Byungkyun; Biswas, Koushik
• Is Part Of: Physical chemistry chemical physics. Volume 19:Issue 40(2017)
• Page Start: 27184
• Page End: 27190
• Publication Date: 2017-08-22
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/c7cp04417h
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : Calculations show that small polarons are unstable in semiconducting hybrid perovskites, whereas shallow traps are possible and likely shape the carrier dynamics. Abstract : There has been considerable speculation over the nature of charge carriers in organic–inorganic hybrid perovskites, i.e., whether they are free and band-like, or they are prone to self-trapping via short range deformation potentials. Unusually long minority-carrier diffusion lengths and moderate-to-low mobilities, together with relatively few deep defects add to their intrigue. Here we implement density functional methods to investigate the room-temperature, tetragonal phase of CH3 NH3 PbI3 . We compare charge localization behavior at shallow levels and associated lattice relaxation versus those at deep polaronic states. The shallow level originates from screened Coulomb interaction between the perturbed host and an excited electron or hole. The host lattice has a tendency towards forming these shallow traps where the electron or hole is localized not too far from the band edge. In contrast, there is a considerable potential barrier that must be overcome in order to initiate polaronic hole trapping. The formation of a hole polaron (I2 − center) involves strong lattice relaxation, including large off-center displacement of the organic cation, CH3 NH3 + . This type of deep polaron is energetically unfavorable, and active shallow traps are expected to shape the carrier dynamics in this material.