Temperature-Dependent Intraband Relaxation of Hybrid Perovskites
Author(s) -
Benjamin T. Diroll
Publication year - 2019
Publication title -
the journal of physical chemistry letters
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 2.563
H-Index - 203
ISSN - 1948-7185
DOI - 10.1021/acs.jpclett.9b02320
Subject(s) - tetragonal crystal system , orthorhombic crystal system , relaxation (psychology) , materials science , crystallite , atmospheric temperature range , condensed matter physics , ultrafast laser spectroscopy , phase transition , jahn–teller effect , chemistry , crystallography , spectroscopy , crystal structure , ion , thermodynamics , psychology , social psychology , physics , quantum mechanics , organic chemistry
Intraband relaxation in polycrystalline films of hybrid perovskites methylammonium lead tribromide and methylammonium lead triiodide are studied by transient absorption spectroscopy from 80 K to >350 K. This temperature range spans the transitions of these materials from the high-temperature cubic phases, intermediate tetragonal phases, and low-temperature orthorhombic phases. The organic cation undergoes a distinct transition from an ordered lattice in the orthorhombic phase to a plastic crystal in cubic and tetragonal phases, which reportedly influences many optoelectronic properties. The much larger exciton binding energy of orthorhombic MAPbI 3 (compared to cubic or tetragonal phases) or MAPbBr 3 substantially changes the transient spectral responses of the materials by reducing the number of free carriers. However, for these measurements at low fluences, both MAPbBr 3 and MAPbI 3 exhibit subpicosecond intraband relaxation over the entire temperature range studied. Intraband relaxation becomes somewhat faster at higher temperatures, but freezing of organic cations are not accompanied by a discontinuity of the intraband relaxation time. These results suggest that configurational freedom of organic cations does not screen carriers from electron-phonon coupling.
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